0806 DSCSA Implementation GFI 2021 - ID of Suspect Product and Notification

Drug Supply Chain
Security Act
Implementation:
Identification of Suspect
Product and Notification
Guidance for Industry

U.S. Department of Health and Human Services
Food and Drug Administration
Center for Drug Evaluation and Research (CDER)
Center for Biologics Evaluation and Research (CBER)
Office of Regulatory Affairs (ORA)
June 2021
Procedural
Revision 1
OMB Control No. 0910-0806
Expiration Date 1/31/2022
See additional PRA statement in section V of this guidance.

Drug Supply Chain Security Act
Implementation: Identification
of Suspect Product and
Notification
Guidance for Industry
Additional copies are available from:
Office of Communications, Division of Drug Information
Center for Drug Evaluation and Research
Food and Drug Administration
10001 New Hampshire Ave., Hillandale Bldg., 4th Floor
Silver Spring, MD 20993-0002
Phone: 855-543-3784 or 301-796-3400; Fax: 301-431-6353
Email: druginfo@fda.hhs.gov
https://www.fda.gov/drugs/guidance-compliance-regulatory-information/guidances-drugs

and/or
Office of Communication, Outreach and Development
Center for Biologics Evaluation and Research
Food and Drug Administration
10903 New Hampshire Ave., Bldg. 71, Room 3128
Silver Spring, MD 20993-0002
Phone: 800-835-4709 or 240-402-8010
Email: ocod@fda.hhs.gov
https://www.fda.gov/vaccines-blood-biologics/guidance-compliance-regulatory-information-biologics/biologics-guidances

U.S. Department of Health and Human Services
Food and Drug Administration
Center for Drug Evaluation and Research (CDER)
Center for Biologics Evaluation and Research (CBER)
Office of Regulatory Affairs (ORA)
June 2021
Procedural
Revision 1

Contains Nonbinding Recommendations
TABLE OF CONTENTS

I.

INTRODUCTION............................................................................................................. 1

II.

BACKGROUND ............................................................................................................... 2

A.

Drug Supply Chain Security Act .................................................................................................. 2

B.

Scope of This Guidance ................................................................................................................. 3

III.
IDENTIFICATION OF SUSPECT PRODUCT AND, FOR MANUFACTURERS,
PRODUCT WITH A HIGH RISK OF ILLEGITIMACY ....................................................... 4
A.

Specific Scenarios That Could Significantly Increase the Risk of a Suspect Product Entering

the Pharmaceutical Distribution Supply Chain ................................................................................... 4
1. Trading Partners and Product Sourcing ......................................................................................... 4
2. Supply, Demand, History, and Value of the Product ....................................................................... 5
3. Appearance of the Product .............................................................................................................. 6
B. Recommendations on How Trading Partners Might Identify Suspect Product and
Determine Whether the Product Is a Suspect Product as Soon as Practicable ................................ 6
C.

For Manufacturers: High Risk of Illegitimacy Notifications ..................................................... 8
1. High Risk of Illegitimacy Notification for Products That the Manufacturer Has Reason To Believe
Are in an Immediate Trading Partner’s Possession............................................................................. 9
2. Specific High Risks That Could Increase the Likelihood of an Illegitimate Product Entering the
U.S. Pharmaceutical Distribution Supply Chain ............................................................................... 10
3. Other High Risks as Determined by FDA: High Risk of Illegitimacy Notification Where a
Manufacturer Has Reason To Believe the Product Has Entered the Pharmaceutical Distribution
Supply Chain ...................................................................................................................................... 11

IV.
NOTIFICATION OF ILLEGITIMATE PRODUCTS AND PRODUCTS WITH A
HIGH RISK OF ILLEGITIMACY .......................................................................................... 12
A.

Notification to FDA ...................................................................................................................... 12

1. Process to Notify FDA of Illegitimate Products ............................................................................ 12
2. Process Used by Manufacturers To Notify FDA of a Product With a High Risk of Illegitimacy .. 13
B. Process for Termination of Notification in Consultation With FDA ...................................... 14

V.

PAPERWORK REDUCTION ACT OF 1995.............................................................. 15

APPENDIX 1: FORM FDA 3911 ............................................................................................. 17

Contains Nonbinding Recommendations

Guidance for Industry 1
Drug Supply Chain Security Act Implementation: Identification of
Suspect Product and Notification
This guidance represents the current thinking of the Food and Drug Administration (FDA or Agency) on
this topic. With the exception of section IV.B, 2 it does not establish any rights for any person and is not
binding on FDA or the public. You can use an alternative approach if it satisfies the requirements of the
applicable statutes and regulations. To discuss an alternative approach, contact the FDA office
responsible for this guidance as listed on the title page.

I.

INTRODUCTION

This guidance is intended to aid trading partners 3,4 (manufacturers, repackagers, wholesale
distributors, and dispensers) in identifying a suspect product as defined at section 581(21) of the
Federal Food, Drug, and Cosmetic Act (FD&C Act) (21 U.S.C. 360eee(21)) and terminating
notifications. As of January 1, 2015, a trading partner that determines a product in its possession
or control is an illegitimate product as defined at section 581(8) of FD&C Act, must notify the
Food and Drug Administration (FDA or Agency) and certain immediate trading partners under
section 582 of the FD&C Act (21 U.S.C. 360eee-1), as added by the Drug Supply Chain Security
Act (DSCSA). Manufacturers are additionally required under section 582 to notify FDA and
certain immediate trading partners, as applicable, after the manufacturer determines or is notified
by FDA or a trading partner that there is a high risk that a suspect product is illegitimate. This
guidance identifies specific scenarios that could significantly increase the risk of a suspect
product entering the pharmaceutical distribution supply chain; provides recommendations on
how trading partners can identify a product and determine whether a product is a suspect product
as soon as practicable; and sets forth the process by which trading partners should notify FDA of
illegitimate product or products with a high risk of illegitimacy, and how they must terminate the
notifications, in consultation with FDA, pursuant to section 582(h)(2)(A).
1

This guidance has been prepared by the Office of Compliance in the Center for Drug Evaluation and Research in
cooperation with the Center for Biologics Evaluation and Research and the Office of Regulatory Affairs at the Food
and Drug Administration.

2

Congress gave FDA authority to implement through binding guidance the process for terminating notifications of
illegitimate product in consultation with FDA. Thus, the discussion of the termination process in section IV has a
binding effect.

3

For this guidance, trading partner is defined in section 581(23)(A) of the Federal Food, Drug, and Cosmetic Act
(21 U.S.C. 360eee(23)(A)), and refers to a manufacturer, repackager, wholesale distributor, or dispenser. For
purposes of this guidance, trading partner does not refer to a third-party logistics provider (3PL) as defined in
section 581(23)(B) of the FD&C Act (21 U.S.C. 360eee(23)(B)), though FDA encourages 3PLs to follow the
recommendations in this guidance to the extent relevant to the 3PL’s operations.
4

Trading partners must be authorized as defined in section 581(2) of the FD&C Act and required under section
582(b)(3), (c)(3), (d)(3), and (e)(3) of the FD&C Act.

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Contains Nonbinding Recommendations

This guidance does not address all provisions of the DSCSA related to suspect and illegitimate
products. As FDA works to implement other provisions of the DSCSA, the Agency intends to
issue additional information to support efforts to develop standards, issue guidance and
regulations, establish pilot programs, and conduct public meetings.
The contents of this document do not have the force and effect of law and are not meant to bind the
public in any way, unless specifically incorporated into a contract. This document is intended only to
provide clarity to the public regarding existing requirements under the law. FDA guidance
documents, including this guidance, should be viewed only as recommendations, unless specific
regulatory or statutory requirements are cited. The use of the word should in Agency guidances
means that something is suggested or recommended, but not required.

An exception to that framework derives from section 582(h)(2)(A) of the Federal Food, Drug,
and Cosmetic Act (FD&C Act), wherein Congress granted authorization to FDA to implement
the process for terminating notifications of illegitimate product in consultation with FDA through
guidance. Accordingly, insofar as this guidance establishes the processes for terminating
notifications of illegitimate product, this document is not subject to the usual restriction in the
above paragraph or in FDA’s good guidance practice regulations that guidances not establish
legally enforceable responsibilities. See 21 CFR 10.115(d). Therefore, section IV.B of this
guidance, which sets forth the process by which trading partners must terminate notifications of
illegitimate product and products with a high risk of illegitimacy in consultation with FDA, has
binding effect, where indicated by the use of the words must, shall, or required.

II.

BACKGROUND
A.

Drug Supply Chain Security Act

On November 27, 2013, the DSCSA (Title II of Public Law 113-54) was signed into law.
Section 203 of the DSCSA added section 582(h)(2) to the FD&C Act, which requires FDA to
issue guidance to aid trading partners in identifying a suspect product and terminating
notifications. Suspect product is defined in section 581(21) of the FD&C Act as a product for
which there is reason to believe it (A) is potentially counterfeit, diverted, or stolen; (B) is
potentially intentionally adulterated such that the product would result in serious adverse health
consequences or death to humans; (C) is potentially the subject of a fraudulent transaction; or
(D) appears otherwise unfit for distribution such that the product would result in serious adverse
health consequences or death to humans. Section 582 of the FD&C Act requires trading
partners, upon determining that a product in their possession or control is a suspect product, to
quarantine the product while they promptly conduct an investigation to determine whether the
product is an illegitimate product. Illegitimate product is defined in section 581(8) of the FD&C
Act as a product for which credible evidence shows that it is (A) counterfeit, diverted, or stolen;
(B) intentionally adulterated such that the product would result in serious adverse health
consequences or death to humans; (C) is the subject of a fraudulent transaction; or (D) appears

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Contains Nonbinding Recommendations
otherwise unfit for distribution such that the product would be reasonably likely to result in
serious adverse health consequences or death to humans. 5
Section 582 of the FD&C Act requires trading partners, upon determining that a product in their
possession or control is illegitimate, to notify FDA and all immediate trading partners (that they
have reason to believe may have received the illegitimate product) not later than 24 hours after
making the determination. FDA anticipates that the immediate trading partners to notify would
include those to whom a trading partner has sold the drugs and in some cases, from whom a
trading partner purchased the drugs. Manufacturers are additionally required under section
582(b)(4)(B)(ii)(II) to notify FDA and immediate trading partners (that the manufacturer has
reason to believe may possess a product manufactured by or purported to be manufactured by the
manufacturer) not later than 24 hours after the manufacturer determines or is notified by FDA or
a trading partner that there is a high risk that the suspect product is illegitimate.
The DSCSA outlines critical steps to build an electronic, interoperable system over a 10-year
period that will identify and trace certain prescription drugs as they are distributed within the
United States. For many years, FDA has been engaged in efforts to improve the security of the
drug supply chain to protect U.S. patients from unsafe, ineffective, and poor quality drugs. Since
at least the formation of the first FDA Counterfeit Drug Task Force in 2003, FDA has strongly
supported a multilayered approach to securing the supply chain. A key component of that
approach has been to encourage heightened vigilance and awareness among supply chain
partners. The electronic, interoperable system that will be established under the DSCSA will
enhance FDA’s ability to help protect U.S. consumers by improving detection and removal of
potentially dangerous drugs from the drug supply chain.
B.

Scope of This Guidance

Pursuant to section 582(h)(2) of the FD&C Act, this guidance identifies specific scenarios that
could significantly increase the risk of a suspect product entering the pharmaceutical distribution
supply chain; provides recommendations on how trading partners can identify such product and
determine whether a product is a suspect product as soon as practicable; describes when
manufacturers should notify FDA of a high risk that a suspect product is illegitimate; and sets
forth the process by which trading partners must terminate notifications in consultation with
FDA regarding illegitimate product under section 582(b)(4)(B)(iv), (c)(4)(B)(iv), (d)(4)(B)(iv),
and (e)(4)(B)(iv) of the FD&C Act and the process for terminating notifications in consultation
with FDA regarding products with a high risk of illegitimacy under section 582(b)(4)(B)(iv).
This guidance also addresses how trading partners should notify FDA when they determine that a
product in their possession or control is an illegitimate product under section 582(b)(4)(B)(ii)(I),
(c)(4)(B)(ii), (d)(4)(B)(ii), and (e)(4)(B)(ii) of the FD&C Act, and how manufacturers should
notify FDA regarding products with a high risk of illegitimacy under section 582(b)(4)(B)(ii)(II).

5

For additional definitions applicable to this guidance, please refer to section 581 of the FD&C Act.

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Contains Nonbinding Recommendations
III.

IDENTIFICATION OF SUSPECT PRODUCT AND, FOR MANUFACTURERS,
PRODUCT WITH A HIGH RISK OF ILLEGITIMACY

Trading partners, upon determining that a product in their possession or control is suspect or
upon receiving a request for verification from FDA (whereby FDA has made a determination
that a product within the possession or control of the trading partner is a suspect product), must
have systems in place that enable them to quarantine suspect product and promptly conduct an
investigation, in coordination with other trading partners, as applicable, to determine whether a
suspect product is illegitimate. 6
As trading partners conduct business on a daily basis, they should exercise vigilance, maintain
awareness about questionable activity or potential threats to their supply chain, and devote
attention and effort to detecting suspect product.
The next two sections of this guidance (A.) identify some specific scenarios that could
significantly increase the risk of suspect products entering the pharmaceutical distribution supply
chain and (B.) make recommendations to assist trading partners in identifying suspect product
and making determinations about whether a product is suspect as soon as practicable. The
scenarios contained in this guidance are based on Agency experience with suspect product in the
drug supply chain. These examples are illustrative and should not be viewed as an exhaustive list
of all potential scenarios that increase the likelihood that a suspect product could enter the
pharmaceutical distribution supply chain. Trading partners should consider the surrounding
circumstances of any particular scenario they may encounter in determining whether a product is
suspect, including whether multiple scenarios are present in any given transaction.
A.

Specific Scenarios That Could Significantly Increase the Risk of a Suspect
Product Entering the Pharmaceutical Distribution Supply Chain

There may be situations involving trading partners where heightened vigilance would be
appropriate. In addition, there could be identifiable characteristics of products that might increase
the likelihood that they are suspect products. The following are examples of some specific
scenarios that could significantly increase the risk of a suspect product entering the drug supply
chain. Thus, trading partners should be particularly diligent when engaging in transactions that
involve:

6

1.

Trading Partners and Product Sourcing

•

Purchasing from a source new to the trading partner.

•

Receiving an unsolicited sales offer from an unknown source. Trading partners
might receive unsolicited offers or advertisements through an email, a fax, a
telephone call, or an in-person sales call from a person or entity with whom they
do not have an established business relationship.

See section 582(b)(4)(A)(i), (c)(4)(A)(i), (d)(4)(A)(i), and (e)(4)(A)(i) of the FD&C Act.

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Contains Nonbinding Recommendations
•

Purchasing on the Internet from an unknown source. Trading partners might be
searching for a better price on the Internet or for a product that they cannot obtain
from their usual source, and might be tempted to turn to a person or entity with
whom they do not have an established business relationship.

•

Purchasing from a source that a trading partner knows or has reason to believe has
engaged in questionable business practices that could increase the risk of suspect
product entering the supply chain, such as:
- A trading partner that has been involved in business transactions where they
sold or delivered illegitimate product.
- A trading partner that has a history of problematic or potentially false
transaction histories, such as those that contain misspelled words or
incomplete information.
- A trading partner that is reluctant to provide a transaction history associated
with the product being purchased, or does not do so in a timely manner.
- A trading partner that provides transaction information, a transaction
statement, and/or transaction history that appears to be incomplete or
questionable.

2.

Supply, Demand, History, and Value of the Product

•

Product that is generally in high demand in the U.S. market.

•

Product that is in higher demand because of its potential or perceived relationship
to a public health or other emergency (e.g., antiviral drugs).

•

Product that has a high sales volume or price in the United States.

•

Product offered at a price that is “too good to be true.”

•

Product that has been previously or is currently being counterfeited or diverted
(e.g., HIV, antipsychotic, or cancer drugs).

•

Product that has been previously or is currently the subject of a drug shortage (see
a list of current drugs in shortage at
http://www.fda.gov/BiologicsBloodVaccines/SafetyAvailability/Shortages/default
.htm and https://www.accessdata.fda.gov/scripts/drugshortages/default.cfm for
more information).

•

Product that has been or is the subject a public alert or announcement related to
drug quality issued by a trading partner or FDA.

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Contains Nonbinding Recommendations
•

Product that has been or is the subject of an FDA counterfeit or cargo theft alert
(See
http://www.fda.gov/drugs/resourcesforyou/consumers/buyingusingmedicinesafely
/counterfeitmedicine/default.htm and
http://www.fda.gov/iceci/criminalinvestigations/ucm182888.htm for more
information).

3.

Appearance of the Product

•

Appearance of a package or a container used for transport (e.g., case or tote) that
seems questionable (e.g., it has a label that contains misspellings or appears
different from the standard label for that product in color, font, images, or
otherwise).

•

Package that exhibits unusual or excessive adhesive residue.

•

Package that contains foreign identification features (such as a different drug
identification number where a National Drug Code (NDC) number would be
expected).

•

Package that is missing information, such as the lot number or other lot
identification, or the expiration date.

•

Package that is missing security or anti-counterfeiting technologies normally
featured on the FDA-approved product that are easily visible to the eye, such as
holograms, color shifting inks, neckbands, or watermarks.

•

Finished dosage form that seems questionable (e.g., it has a different shape or
color from the FDA-approved product, a different or unusual imprint, an unusual
odor, or there are signs of poor quality like chips or cracks in tablet coatings or
smeared or unclear ink imprints).

B.

Recommendations on How Trading Partners Might Identify Suspect Product
and Determine Whether the Product Is a Suspect Product as Soon as
Practicable

The following are recommendations for trading partners, as applicable, on ways that they can
expeditiously identify suspect product and determine whether the product is suspect (and, after
investigation, whether it is illegitimate). In general, trading partners should exercise due
diligence and shall only conduct business with authorized trading partners. 7 Trading partners
should discuss with each other any observations, questions, or concerns they have related to the
status of a drug as a suspect product to aid them in determining whether the drug should be
considered a suspect product. Because a product’s manufacturer is usually the best able to assess
7

See section 582(b)(3), (c)(3), (d)(3), and (e)(3) of the FD&C Act.

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Contains Nonbinding Recommendations
the authenticity and quality of a product, a trading partner should consult with the manufacturer
when conducting any investigation of suspect product. Trading partners should also contact
regulatory authorities, law enforcement, or other available resources to aid in that determination
when additional expertise is called for to make an accurate assessment of the status of a drug as a
suspect product. If a trading partner receives a product in a secured transport container or sealed
homogenous case, trading partners should examine the appearance of that container as
recommended below. If trading partners observe anything questionable, they should take steps to
ascertain whether the product inside the transport container is suspect. Strategies to identify
suspect product include, but are not limited to, the following recommendations:
•

Be alert for offers of product for sale at a very low price or one that is “too good
to be true.”

•

Closely examine the package and the transport container (such as the case or
tote):
- To look for signs that it has been compromised (e.g., opened, broken seal,
damaged, repaired, or otherwise altered). If a trading partner receives a
product in a secured transport container or sealed homogenous case, trading
partners should examine the appearance of that container to see if anything
about that appearance seems questionable, such as shrink wrap that has
unexpected markings, or a seal that is broken, torn, or repaired. Such
examinations may include:


Seeing if the package or the transport container has changed since the last
shipment of the same product type was received for an unexplained reason
(e.g., a notification about the change from the manufacturer has not been
received).



Seeing if product inserts are missing, do not correspond to the product, or
are questionable in some way.

- For shipping addresses, postmarks, or other materials indicating that the
product came from an unexpected foreign entity or source.
•

Closely examine the label on the package, and the label on the individual retail
unit, if applicable, for:
- Any missing information, such as the lot number or other lot identification,
NDC, or strength of the drug.
- Any altered product information, such as smudged print or print that is very
difficult to read.
- Misspelled words.
- Bubbling in the surface of a label.

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Lack of an “Rx only” symbol. 8
Foreign language with little or no English provided. 9
Foreign language that is used to describe the lot number. 10
A product name that differs from the name that appears on the FDA-approved
drug label or labeling.
- A product name that is the product name for a foreign version of the drug.
- A product that is transported in a case or tote, when not expected under the
circumstances.
- Lot numbers and expiration dates on product that do not match the lot
numbers and expiration dates of its outer container.
-

Again, under section 582 of the FD&C Act, trading partners must have systems in place that
enable them, upon determining that a product in their possession or control is suspect or upon
receiving a request for verification from the FDA that has made a determination that a product
within the possession or control of the trading partner is a suspect product, to quarantine suspect
product and promptly conduct an investigation, in coordination with the manufacturer and other
trading partners, as applicable, to determine whether a suspect product is illegitimate. In
addition, trading partners must, as applicable, make the notifications described in section
582(b)(4)(B)(ii)(I), (c)(4)(B)(ii), (d)(4)(B)(ii), and (e)(4)(B) of the FD&C Act related to
illegitimate product determinations and, for manufacturers, the notification of a high risk of
illegitimacy described in section 582(b)(4)(B)(ii)(II).
C.

For Manufacturers: High Risk of Illegitimacy Notifications

Section 582(b)(4)(B)(ii)(II) of the FD&C Act requires manufacturers to make notifications in
certain circumstances for suspect products that pose a high risk of illegitimacy. The provision
states as follows:
(II) HIGH RISK OF ILLEGITIMACY.--A manufacturer shall notify the Secretary and
immediate trading partners that the manufacturer has reason to believe may have in the
trading partner’s possession a product manufactured by, or purported to be a product
manufactured by, the manufacturer not later than 24 hours after determining or being
notified by the Secretary or a trading partner that there is a high risk that such product is
an illegitimate product. For purposes of this subclause, a ‘high risk’ may include a
specific high risk that could increase the likelihood that illegitimate product will enter the
pharmaceutical distribution supply chain and other high risks as determined by the
Secretary in guidance pursuant to subsection (h).

While suspect product generally does not require notification, FDA interprets this provision to
require manufacturers to notify (1) FDA and (2) the manufacturer’s immediate trading partners
8
Or, for products distributed solely in the Commonwealth of Puerto Rico or any other territory where the
predominant language is Spanish, “Solamente Rx” (21 CFR 201.16).
9

Except for products distributed solely in the Commonwealth of Puerto Rico or any other territory where the
predominant language is one other than English (21 CFR 201.15 (c)(1)).

10

Except for products distributed solely in the Commonwealth of Puerto Rico or any other territory where the
predominant language is one other than English (21 CFR 201.15(c)(1)).

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Contains Nonbinding Recommendations
(that the manufacturer has reason to believe may have in the trading partner’s possession a
product manufactured by, or purported to be a product manufactured by, the manufacturer)
where the circumstances surrounding the suspect product include at least one of three types of
high risk factors described below:
(1) Within 24 hours after determining or being notified by FDA or a trading partner that
there is a high risk that a product that the manufacturer has reason to believe is in an
immediate trading partner’s possession is an illegitimate product.
(2) Within 24 hours after determining or being notified by FDA or a trading partner that
there is a specific high risk that could increase the likelihood that illegitimate product
will enter the U.S. pharmaceutical distribution supply chain.
(3) Within 24 hours after determining or being notified by FDA or a trading partner that
there exists an “other high risk” as determined by FDA in guidance pursuant to
subsection 582(h).
FDA believes that Congress intended section 582(b)(4)(B)(ii)(II) to give flexibility to
manufacturers to determine systems and processes needed for verification, including the
surveillance systems that many manufacturers already have in place to detect counterfeit and
otherwise violative versions of their products. Manufacturers may discover product with a high
risk of illegitimacy either through their own investigation of suspect product, or through
information they receive from a variety of other sources, including from within their own
company, from their trading partners, from FDA, or from other domestic and/or foreign
regulatory authorities.
Below are scenarios and examples in which a manufacturer should make a notification under
section 582(b)(4)(B)(ii)(II).
1.

High Risk of Illegitimacy Notification for Products That the Manufacturer Has
Reason To Believe Are in an Immediate Trading Partner’s Possession

The first general scenario involves notifications for products that the manufacturer has reason to
believe are in an immediate trading partner’s possession.
An example of this scenario might occur when the manufacturer is asked to coordinate a suspect
product investigation by an immediate trading partner under section 582(c)(4)(B), (d)(4)(B), or
(e)(4)(B), and the manufacturer determines that there is a high risk that the suspect product is
illegitimate. Some sample scenarios involving high risks of illegitimacy, in which a manufacturer
should make a notification, include:
•

A manufacturer learns from a trading partner that a suspect product purporting to be one
produced by that manufacturer has been found in the U.S. pharmaceutical distribution
supply chain. The manufacturer examines the suspect product and believes the product
has a high risk of being illegitimate but wants to take additional steps before determining
that it is illegitimate. The manufacturer has reason to believe that additional high risk

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products are in the possession of immediate trading partners. For example, a wholesale
distributor informs a manufacturer that it believes it has a counterfeit of that
manufacturer’s product. The wholesale distributor sends the product to the manufacturer.
The manufacturer examines the product and believes it could be counterfeit, but wants to
perform a laboratory analysis or other analysis for confirmation.
•

A manufacturer learns that its product has been stolen or diverted in the United States. As
the manufacturer is investigating the validity of the claim that the product is stolen or
diverted, the manufacturer has reason to believe that an immediate trading partner has the
potentially stolen or diverted product in its possession.
2.

Specific High Risks That Could Increase the Likelihood of an Illegitimate Product
Entering the U.S. Pharmaceutical Distribution Supply Chain

Section 582(b)(4)(B)(ii)(II) states that a high risk of illegitimacy may include a “specific high
risk” that could increase the likelihood that illegitimate product will enter the U.S.
pharmaceutical distribution supply chain. In such cases, the product has not yet entered the
pharmaceutical distribution supply chain, so no immediate trading partners would have it in their
possession. Section 582(b)(4)(B)(ii)(II) thus would require the manufacturer to make a
notification to FDA, but the manufacturer would not be required to notify immediate trading
partners. However, while not required, a manufacturer may notify its immediate trading partners
of such “specific high risk[s]” to help ensure the integrity of the supply chain. Some examples
involving specific high risks include:
•

A manufacturer learns that a product with a high risk of illegitimacy (purporting to be
one produced by that manufacturer) has been found in another country, and that such
product is likely destined for a trading partner in the United States. For instance, the
manufacturer learns from a foreign regulatory authority that one of its products has been
counterfeited in another country, and that some of that product is on a cargo ship destined
for the United States for delivery to a wholesale distributor.

•

A manufacturer learns that its product was stolen or diverted in another country, and that
such product is destined for the United States in a manner that leads the manufacturer to
believe the product will likely enter the U.S. pharmaceutical distribution supply chain.
For instance, the manufacturer learns from a foreign law enforcement agency that its
product was stolen during transport in another country and is on a plane destined for the
United States for delivery to a dispenser.

•

A manufacturer learns that there is a high risk that its product has been intentionally
adulterated in another country such that the product would result in serious adverse health
consequences or death to humans, and that such product is likely destined for the United
States in a manner that leads the manufacturer to believe the product will enter the
pharmaceutical distribution supply chain. For instance, the manufacturer learns from its
own investigation that there is a high risk that a contaminant that would result in serious
adverse health consequences or death to humans was added to a product in another
country and sent to a repackager in the United States.

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As noted above, the scenarios given in sections 1 and 2 are examples, rather than an exhaustive
list of circumstances in which trading partners should make notifications under section
582(b)(4)(B)(ii)(II).
3.

Other High Risks as Determined by FDA: High Risk of Illegitimacy Notification
Where a Manufacturer Has Reason To Believe the Product Has Entered the
Pharmaceutical Distribution Supply Chain

Section 582(b)(4)(B)(ii)(II) of the FD&C Act permits FDA to determine, through guidance
pursuant to section 582(h), “other high risks” that would trigger a notification under this
provision. FDA believes that one “other high risk” not covered by the two general scenarios
described above is when a manufacturer has reason to believe that an illegitimate product has
entered the pharmaceutical distribution supply chain, even though the manufacturer does not
have reason to believe that an immediate trading partner possesses the high risk product. 11 As
with the second general scenario, described above, section 582(b)(4)(B)(ii)(II) would require the
manufacturer to make a notification to FDA, but the manufacturer would not be required to
notify immediate trading partners. To help ensure the integrity of the supply chain, however,
FDA recommends that a manufacturer notify its immediate trading partners of this “other high
risk,” even if that manufacturer does not have reason to believe that its immediate trading
partners may have the high risk product in their possession.
A manufacturer could learn that a product with a high risk of illegitimacy that was manufactured
by (or purported to be manufactured by) that manufacturer, may be in the possession of a trading
partner, but that trading partner is not an immediate trading partner of the manufacturer. Some
examples that involve this other high risk include:

11

•

A manufacturer learns that a licensed health care practitioner is administering an
oncology drug to patients that purports to have been manufactured by that manufacturer,
but the manufacturer determines that there is a high risk that the drug is a counterfeit. The
licensed health care practitioner purchased the drug from a wholesale distributor, so
he/she is not an immediate trading partner of the manufacturer. However, the
manufacturer believes that the product has entered the pharmaceutical distribution supply
chain.

•

A manufacturer learns that its product has been stolen or diverted in the United States,
and the manufacturer learns that a patient filled a prescription and received some of the
stolen or diverted product. The patient suffers an adverse event, and FDA and the
manufacturer are notified of that situation. Because the dispenser did not purchase the
product from the manufacturer, it is not an immediate trading partner of the
manufacturer. However, the product has entered the pharmaceutical distribution supply
chain.

•

A manufacturer learns that wholesale distributor B received product and transaction
history going back to the manufacturer from wholesale distributor A, but the listed

FDA reserves authority to articulate additional “other high risk[s]” in subsequent guidance(s).

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Contains Nonbinding Recommendations
dosage form of the product on the transaction history is not one that has ever been used
by the manufacturer. Wholesale distributor B provided a copy of the transaction history it
received from wholesale distributor A to the manufacturer, and the manufacturer
concluded, after reviewing the copy and receiving similar reports from other trading
partners, that a fraudulent transaction had occurred. Because wholesale distributor B did
not purchase the product from the manufacturer, it is not an immediate trading partner of
the manufacturer. However, the product has entered the pharmaceutical distribution
supply chain.

IV.

NOTIFICATION OF ILLEGITIMATE PRODUCTS AND PRODUCTS WITH A
HIGH RISK OF ILLEGITIMACY
A.

Notification to FDA

As discussed above, trading partners must, as applicable, make the notifications described in
section 582(b)(4)(B)(ii)(I), (c)(4)(B)(ii), (d)(4)(B)(ii), and (e)(4)(B)(ii) of the FD&C Act related
to illegitimate product determinations and, for manufacturers, the notification of a high risk of
illegitimacy described in section 582(b)(4)(B)(ii)(II). This section of the guidance addresses the
process by which trading partners should notify FDA and other trading partners regarding
illegitimate products under section 582. After review of the circumstances surrounding the event,
if FDA determines that notification is not required under section 582(b)(4)(B)(ii)(I), (c)(4)(B)(ii),
(d)(4)(B)(ii), (e)(4)(B)(ii), or (b)(4)(B)(ii)(II) of the FD&C Act, FDA intends to inform the
submitting entity.
1.

Process to Notify FDA of Illegitimate Products

The following process should be used to notify FDA of illegitimate products:
(1) Trading partners should access FDA’s web page at
http://www.accessdata.fda.gov/scripts/cder/email/drugnotification.cfm for notifications.
(2) Trading partners should follow the instructions on the web page for accessing Form FDA
3911 (Appendix 1). Using this form, trading partners should provide information about
the person or entity initiating the notification, the product determined to be illegitimate
that is the subject of the notification to FDA, and a description of the circumstances
surrounding the event that prompted the notification.
(3) Form FDA 3911 should be submitted using the method provided in the form or on the
web page.
(4) FDA will acknowledge receipt of the notification and assign an incident number. This
number should be referenced in all future correspondence about the illegitimate product,
including any request for termination.

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Contains Nonbinding Recommendations
(5) In addition to notifying FDA, the trading partner that determines it has an illegitimate
product in its possession or control must notify all immediate trading partners that it has
reason to believe may have received the illegitimate product. Trading partners may notify
other trading partners of an illegitimate product using existing systems and processes
used for similar types of communications to those partners, which might include, but are
not limited to, posting of notifications on a company website, telephoning, sending an
email, or mailing or faxing a notification.
2.

Process Used by Manufacturers To Notify FDA of a Product With a High Risk of
Illegitimacy

The following process should be used by manufacturers to notify FDA of a product with a high
risk of illegitimacy, under section 582(b)(4)(B)(ii)(II):
(1) Manufacturers should access FDA’s web page at
http://www.accessdata.fda.gov/scripts/cder/email/drugnotification.cfm
(2) Manufacturers should follow the instructions on the web page for accessing Form FDA
3911 (Appendix 1). Using this form, manufacturers should provide information about the
person or entity initiating the notification, the product determined to have a high risk of
illegitimacy that is the subject of the notification to FDA, and a description of the
circumstances surrounding the event that prompted the notification.
(3) FDA will acknowledge receipt of the notification and assign an incident number. This
number should be documented in all future correspondence about the product with the
high risk of illegitimacy, including any request for termination.
(4) In addition to notifying FDA, the manufacturer that determines that a product has a high
risk of illegitimacy must notify all immediate trading partners that it believes may
possess the drug. Manufacturers may notify other trading partners of a product with a
high risk of illegitimacy using existing systems and processes used for similar types of
communications to those partners, which might include, but are not limited to, posting of
notifications on a company website, telephoning, sending an email, or mailing or faxing a
notification.
(5) If a product with a high risk of illegitimacy is found to be an illegitimate product,
manufacturers should submit a follow-up notification that explains the updated
classification and references the incident number of the original notification of high risk
of illegitimacy.
(6) If it is determined that a product that was subject to a high risk of illegitimacy notification
is not an illegitimate product, manufacturers must submit a request for termination of the
high risk of illegitimacy notification to FDA according to the process in section B below.
For a discussion of the terms like counterfeit, diverted, fraudulent transaction, and unfit for
distribution, as they relate to verification obligations (including notification), you may also wish

13

Contains Nonbinding Recommendations
to refer to FDA’s guidance on Definitions of Suspect Product and Illegitimate Product for
Verification Obligations Under the Drug Supply Chain Security Act. 12 Furthermore, this
guidance is intended only to assist trading partners in understanding DSCSA and determining
whether they are required to submit a Form FDA 3911 to FDA. For products outside the scope of
DSCSA, but in violation of other requirements of the FD&C Act, trading partners should report
the violation through the appropriate mechanisms as required under the relevant provisions of the
law. You may contact the CDER’s Division of Supply Chain Integrity for other supply chain
issues related to drugs and components at: DrugSupplyChainIntegrity@fda.hhs.gov.
B.

Process for Termination of Notification in Consultation With FDA 13

Section 582(h)(2)(A) of the FD&C Act directs FDA to issue guidance setting forth the process
that trading partners shall follow for terminating notifications regarding illegitimate product or
for manufacturers, terminating notification of a high risk of illegitimacy, in consultation with
FDA, under section 582(b)(4)(B), (c)(4)(B), (d)(4)(B), and (e)(4)(B). Section 582(b)(4)(B),
(c)(4)(B), (d)(4)(B), and (e)(4)(B) require trading partners to have in place systems to enable
them to terminate notifications, in consultation with FDA. This section of the guidance addresses
the process by which trading partners must terminate such notifications in consultation with
FDA. This process must be used when trading partners believe that a notification they made to
FDA regarding illegitimate product or, for a manufacturer, a notification of a high risk of
illegitimacy is no longer necessary.
The process for terminating notifications in consultation with FDA is as follows:
(1) The trading partner making a notification to the FDA shall be responsible for making the
request for termination.
(2) Trading partners must access FDA’s web page at
http://www.accessdata.fda.gov/scripts/cder/email/drugnotification.cfm for termination of
notifications.
(3) Trading partners must follow the instructions on the web page for accessing Form FDA
3911 (Appendix 1). Using this form, trading partners must provide to FDA information
about the person or entity initiating the request for termination, the illegitimate product or
the product with a high risk of illegitimacy, the notification that was issued, and an
explanation about what actions have taken place or what information has become
available that makes the notification no longer necessary. Trading partners must include
the FDA-assigned incident number associated with the notification in the request for
termination.
12

See the FDA guidance for industry Definitions of Suspect Product and Illegitimate Product for Verification
Obligations Under the Drug Supply Chain Security Act available on the FDA Drugs guidance web page under
Procedural. We update guidances periodically. For the most recent version of a guidance, check the FDA guidance
web page at https://www.fda.gov/regulatory-information/search-fda-guidance-documents.
13
Insofar as section IV.B. of this guidance sets forth the process by which trading partners should terminate
notifications of an illegitimate product or products with a high risk of illegitimacy in consultation with FDA, it has
binding effect.

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Contains Nonbinding Recommendations

(4) This form must be submitted by using the method provided in the form or on the web
page. The trading partner’s submission of a request for termination of a notification will
be viewed as a request for consultation with FDA, as required in section 582 of the
FD&C Act. FDA may request any additional information it determines necessary to
complete the consultation.
(5) FDA will review the request and consult with the trading partner. The response time will
depend on the number of requests for termination and the circumstances surrounding the
requests for termination that are received by FDA.
FDA interprets the DSCSA’s requirement for trading partners to “mak[e] a determination, in
consultation with the Secretary, that a notification is no longer necessary” 14 to require that
trading partners provide the Agency with an opportunity to provide its expert views and advice
on proposed terminations of notifications. Therefore, a trading partner must wait until FDA
responds to the termination request before the trading partner notifies other trading partners that
a notification is terminated. FDA intends to respond to requests for termination within 10
business days of submission. In some cases, FDA may contact a trading partner to notify the
partner that additional time is needed to respond to the request for termination. If a trading
partner believes that exigent circumstances require expedited consideration of a termination
request (e.g., a potential drug shortage), the trading partner must describe those circumstances to
FDA in the termination request on the Form FDA 3911 when making the request for termination.
Under section 582(b)(4)(B), (c)(4)(B), (d)(4)(B), and (e)(4)(B) of the FD&C Act, after FDA
provides its consultation response and the trading partner determines that the notification is no
longer necessary, the trading partner that made the request for termination must promptly notify
immediate trading partners that the notification has been terminated. Trading partners may notify
their trading partners of a termination using existing systems and processes used for similar types
of communications to those partners, which might include, but are not limited to, posting of
notifications on a company website, telephoning, sending an email, or mailing or faxing a letter
or notification.

V.

PAPERWORK REDUCTION ACT OF 1995

This guidance contains information collection provisions that are subject to review by the Office
of Management and Budget (OMB) under the Paperwork Reduction Act of 1995 (44 U.S.C.
3501-3520).
The time required to complete this information collection is estimated to average as follows.
Notify FDA of an Illegitimate Product:
•
14

1 hour for manufacturers and repackagers

Section 582(b)(4)(iv), (c)(4)(B)(iv), (d)(4)(B)(iv), and (e)(4)(B)(iv) of the FD&C Act.

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Contains Nonbinding Recommendations
•
•

1 hour for wholesale distributors
1 hour for dispensers

Notify Trading Partners of an Illegitimate Product or a Product With a High Risk of
Illegitimacy:
•
•
•

0.20 hour (12 minutes) for manufacturers and repackagers
0.20 hour (12 minutes) for wholesale distributors
0.20 hour (12 minutes) for dispensers

Consult With FDA and Terminate Notification:
•
•
•

1 hour for manufacturers and repackagers
1 hour for wholesale distributors
1 hour for dispensers

Notify Trading Partners That a Termination Has Been Terminated:
•
•
•

0.20 hour (12 minutes) for manufacturers and repackagers
0.20 hour (12 minutes) for wholesale distributors
0.20 hour (12 minutes) for dispensers

These estimates include the time to review instructions, gather the data needed, and complete and
review the information collection and transmit to FDA. It also includes the time to notify trading
partners. Send comments regarding this burden estimate or suggestions for reducing this burden
to: Office of Regulatory Policy, Center for Drug Evaluation and Research, Food and Drug
Administration, 10903 New Hampshire Ave., Silver Spring, MD 20993-0002.
An agency may not conduct or sponsor, and a person is not required to respond to, a collection of
information unless it displays a currently valid OMB control number. The OMB control number
for this information collection is 0910-0806 (expires 1/31/2022).

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Contains Nonbinding Recommendations
APPENDIX 1: FORM FDA 3911
FORM FDA 3911 and the FORM FDA 3911 Instructions Supplement are available at
https://www.fda.gov/drugs/drug-supply-chain-security-act-dscsa/drug-notifications-frequentlyasked-questions and the FORM FDA 3911 Instructions Supplement is available at
https://www.fda.gov/downloads/AboutFDA/ReportsManualsForms/Forms/UCM513942.pdf.
If you are experiencing difficulties accessing the form, please contact the FDA forms manager at
FormsManager@OC.FDA.GOV for assistance.

17