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Form Approved: OMB No. 0910-0338
Expiration Date: January 31, 2017
See PRA Statement on page 3.
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
APPLICATION TO MARKET A NEW OR ABBREVIATED NEW
DRUG OR BIOLOGIC FOR HUMAN USE
1. Date of Submission (mm/dd/yyyy)
(Title 21, Code of Federal Regulations, Parts 314 & 601)
2. Name of Applicant
APPLICANT INFORMATION
3. Telephone Number (Include country code if applicable and area code) 4. Facsimile (FAX) Number (Include country
code if applicable and area code)
5. Applicant Address
Address 1 (Street address, P.O. box, company name c/o)
Email Address
Address 2 (Apartment, suite, unit, building, floor, etc.)
City
State/Province/Region
Country
U.S. License Number if previously issued
ZIP or Postal Code
6. Authorized U.S. Agent (Required for non-U.S. applicants)
Authorized U.S. Agent Name
Telephone Number (Include area code)
Address 1 (Street address, P.O. box, company name c/o)
FAX Number (Include area code)
Address 2 (Apartment, suite, unit, building, floor, etc.)
City
State
Email Address
ZIP Code
7. NDA, ANDA, or BLA Application Number
PRODUCT DESCRIPTION
8. Supplement Number (If applicable)
9. Established Name (e.g., proper name, USP/USAN name)
10. Proprietary Name (Trade Name) (If any)
11. Chemical/Biochemical/Blood Product Name (If any)
12. Dosage Form
13. Strengths
15. Proposed Indication for Use
14. Route of Administration
Is this indication for a rare disease (prevalence <200,000 in U.S.)?
Does this product have an FDA
Orphan Designation for this
indication?
Yes
No
16. Application Type
(Select one)
APPLICATION INFORMATION
17. If an NDA, identify the type
505 (b)(1)
If yes, provide the Orphan
Designation number for this
indication:
New Drug Application (NDA)
Yes
No
Contin.
Page for
#15
Biologics License Application (BLA)
Abbreviated New Drug Application (ANDA)
18. If a BLA, identify the type
505 (b)(2)
351 (a)
351 (k)
19. If a 351(k), identify the biological reference product that is the basis for the submission.
Name of Biologic:
Holder of Licensed Application:
20. If an ANDA, or 505(b)(2), identify the listed drug product that is the basis for the submission.
Name of Drug:
Application Number of Relied Upon Product:
Indicate Patent Certification(s):
P1
21. Submission (Select one)
Original
Product Correspondence
P2
P3
P4
Labeling Supplement
REMS Supplement
Section viii - MOU
CMC Supplement
Statement of no relevant patents
Efficacy Supplement
Postmarketing Requirements or Commitments
Annual Report
Periodic Safety Report
Other (Specify):
FORM FDA 356h (1/14)
Page 1 of 3
PSC Publishing Services (301) 443-6740
EF
Previous Page
22. Submission
Sub-Type
Next Page
Presubmission
Amendment
Initial Submission
Resubmission
24. Does this submission contain only pediatric data?
23. If a supplement, identify
the appropriate category.
Yes
CBE
Prior Approval (PA)
CBE-30
No
25. Reasons for Submission
26. Proposed Marketing Status (Select one)
27. This application is (Select one)
Prescription Product (Rx)
Paper
Paper and Electronic
Over-The-Counter Product (OTC)
Electronic
28. Number of Volumes Submitted
29. Establishment Information (Full establishment information should be provided in the body of the application.)
Refer to the instruction sheet (Form FDA 356h Supplement) for more information.
Establishment Name
Address 1 (Street address, P.O. box, company name c/o)
Registration (FEI) Number
Address 2 (Apartment, suite, unit, building, floor, etc.)
MF Number
State/Province/Region
City
Country
ZIP or Postal Code
Is the establishment new to the application?
Yes
Establishment DUNS Number
What is the status of the establishment?
Pending
Active
No
Inactive
Withdrawn
Establishment Contact Information
Name of Contact for the Establishment
Telephone Number (Include area code)
Address 1 (Street address, P.O. box, company name c/o)
FAX Number (Include area code)
Address 2 (Apartment, suite, unit, building, floor, etc.)
City
State/Province/Region
Country
Email Address
ZIP or Postal Code
Is the site ready
Yes
for inspection?
If No, when will site be
ready? (mm/dd/yyyy)
Manufacturing Steps and/or Type of Testing
No
N/A
Continuation Page for #29
30. Cross References (List related BLAs, INDs, NDAs, PMAs, 510(k)s, IDEs, BMFs, MAFs, and DMFs referenced in the current application.)
Contin.
Page for
#30
31. This application contains the following items (Select all that apply)
1. Index
2. Labeling (Select one):
4. Chemistry Section
Draft Labeling
Final Printed Labeling
3. Summary (21 CFR 314.50 (c))
A. Chemistry, manufacturing, and controls information (e.g., 21 CFR 314.50(d)(1); 21 CFR 601.2)
B. Samples (21 CFR 314.50 (e)(1); 21 CFR 601.2 (a)) (Submit only upon FDA’s request)
C. Methods validation package (e.g., 21 CFR 314.50(e)(2)(i); 21 CFR 601.2)
5. Nonclinical pharmacology and toxicology section
(e.g., 21 CFR 314.50(d)(2); 21 CFR 601.2)
6. Human pharmacokinetics and bioavailability section
(e.g., 21 CFR 314.50(d)(3); 21 CFR 601.2)
7. Clinical microbiology section (e.g., 21 CFR 314.50(d)(4))
8. Clinical data section (e.g., 21 CFR 314.50(d)(5); 21 CFR 601.2)
Item 31 continued on page 3
FORM FDA 356h (1/14)
Page 2 of 3
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31. This application contains the following items (Continued; select all that apply)
9. Safety update report (e.g., 21 CFR 314.50(d)(5)(vi)(b);
21 CFR 601.2)
10. Statistical section (e.g., 21 CFR 314.50(d)(6); 21 CFR 601.2)
11. Case report tabulations (e.g., 21 CFR 314.50(f)(1);
21 CFR 601.2)
12. Case report forms (e.g., 21 CFR 314.50 (f)(2); 21 CFR 601.2)
13. Patent information on any patent that claims the drug/
biologic (21 U.S.C. 355(b) or (c))
14. A patent certification with respect to any patent that claims the
drug/biologic (21 U.S.C. 355 (b)(2) or (j)(2)(A))
15. Establishment description (21 CFR Part 600, if applicable)
16. Debarment certification (FD&C Act 306 (k)(1))
17. Field copy certification (21 CFR 314.50 (l)(3))
18. User Fee Cover Sheet (PDUFA Form FDA 3397, GDUFA Form
FDA 3794, BsUFA Form FDA 3792, or MDUFMA Form FDA 3601)
19. Financial Disclosure Information (21 CFR Part 54)
20. Other (Specify):
CERTIFICATION
I agree to update this application with new safety information about the product that may reasonably affect the statement of contraindications,
warnings, precautions, or adverse reactions in the draft labeling. I agree to submit safety update reports as provided for by regulation or as
requested by FDA. If this application is approved, I agree to comply with all applicable laws and regulations that apply to approved applications,
including, but not limited to, the following:
1. Good manufacturing practice regulations in 21 CFR Parts 210, 211 or applicable regulations, Parts 606, and/or 820.
2. Biological establishment standards in 21 CFR Part 600.
3. Labeling regulations in 21 CFR Parts 201, 606, 610, 660, and/or 809.
4. In the case of a prescription drug or biological product, prescription drug advertising regulations in 21 CFR Part 202.
5. Regulations on making changes in application in FD&C Act section 506A, 21 CFR 314.71, 314.72, 314.97, 314.99, and 601.12.
6. Regulations on Reports in 21 CFR 314.80, 314.81, 600.80, and 600.81.
7. Local, state, and Federal environmental impact laws.
If this application applies to a drug product that FDA has proposed for scheduling under the Controlled Substances Act, I agree not to market
the product until the Drug Enforcement Administration makes a final scheduling decision.
The data and information in this submission have been reviewed and, to the best of my knowledge, are certified to be true and accurate.
Warning: A willfully false statement is a criminal offense, U.S. Code, title 18, section 1001.
32. Typed Name and Title of Applicant’s Responsible Official
34. Telephone Number (Include country
code if applicable and area code)
33. Date (mm/dd/yyyy)
35. FAX Number (Include country code if
applicable and area code)
36. Email Address
37. Address of Applicant’s Responsible Official
Address 1 (Street address, P.O. box, company name c/o)
Address 2 (Apartment, suite, unit, building, floor, etc.)
City
State/Province/Region
Country
ZIP or Postal Code
38. Signature of Applicant’s Responsible Official or
Other Authorized Official
Sign
39. Countersignature of Authorized U.S. Agent
Sign
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FORM FDA 356h (1/14)
Page 3 of 3
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FIRST CONTINUATION PAGE FOR ITEM 15 – Proposed Indication for Use
Please fill out as many sets of answers as needed, completing all elements within each set that you start.
Proposed Indication for Use
Is this indication for a rare disease (prevalence <200,000 in U.S.)?
Does this product have an FDA
Orphan Designation for this
indication?
Yes
No
Proposed Indication for Use
Proposed Indication for Use
Proposed Indication for Use
Proposed Indication for Use
Proposed Indication for Use
Proposed Indication for Use
Proposed Indication for Use
Proposed Indication for Use
Remove Continuation Page
FORM FDA 356h (1/14)
Yes
No
Yes
No
Yes
No
Yes
No
Yes
No
If yes, provide the Orphan
Designation number for this
indication:
Is this indication for a rare disease (prevalence <200,000 in U.S.)?
Does this product have an FDA
Orphan Designation for this
indication?
Yes
No
No
If yes, provide the Orphan
Designation number for this
indication:
Is this indication for a rare disease (prevalence <200,000 in U.S.)?
Does this product have an FDA
Orphan Designation for this
indication?
Yes
No
Yes
If yes, provide the Orphan
Designation number for this
indication:
Is this indication for a rare disease (prevalence <200,000 in U.S.)?
Does this product have an FDA
Orphan Designation for this
indication?
Yes
No
No
If yes, provide the Orphan
Designation number for this
indication:
Is this indication for a rare disease (prevalence <200,000 in U.S.)?
Does this product have an FDA
Orphan Designation for this
indication?
Yes
No
Yes
If yes, provide the Orphan
Designation number for this
indication:
Is this indication for a rare disease (prevalence <200,000 in U.S.)?
Does this product have an FDA
Orphan Designation for this
indication?
Yes
No
No
If yes, provide the Orphan
Designation number for this
indication:
Is this indication for a rare disease (prevalence <200,000 in U.S.)?
Does this product have an FDA
Orphan Designation for this
indication?
Yes
No
Yes
If yes, provide the Orphan
Designation number for this
indication:
Is this indication for a rare disease (prevalence <200,000 in U.S.)?
Does this product have an FDA
Orphan Designation for this
indication?
Yes
No
No
If yes, provide the Orphan
Designation number for this
indication:
Is this indication for a rare disease (prevalence <200,000 in U.S.)?
Does this product have an FDA
Orphan Designation for this
indication?
Yes
No
Yes
If yes, provide the Orphan
Designation number for this
indication:
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SECOND CONTINUATION PAGE FOR ITEM 15 – Proposed Indication for Use
Please fill out as many sets of answers as needed, completing all elements within each set that you start.
Proposed Indication for Use
Is this indication for a rare disease (prevalence <200,000 in U.S.)?
Does this product have an FDA
Orphan Designation for this
indication?
Yes
No
Proposed Indication for Use
Proposed Indication for Use
Proposed Indication for Use
Proposed Indication for Use
Proposed Indication for Use
Proposed Indication for Use
Proposed Indication for Use
Proposed Indication for Use
Remove Continuation Page
FORM FDA 356h (1/14)
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Page X of X
Yes
No
Yes
No
Yes
No
Yes
No
Yes
No
If yes, provide the Orphan
Designation number for this
indication:
Is this indication for a rare disease (prevalence <200,000 in U.S.)?
Does this product have an FDA
Orphan Designation for this
indication?
Yes
No
No
If yes, provide the Orphan
Designation number for this
indication:
Is this indication for a rare disease (prevalence <200,000 in U.S.)?
Does this product have an FDA
Orphan Designation for this
indication?
Yes
No
Yes
If yes, provide the Orphan
Designation number for this
indication:
Is this indication for a rare disease (prevalence <200,000 in U.S.)?
Does this product have an FDA
Orphan Designation for this
indication?
Yes
No
No
If yes, provide the Orphan
Designation number for this
indication:
Is this indication for a rare disease (prevalence <200,000 in U.S.)?
Does this product have an FDA
Orphan Designation for this
indication?
Yes
No
Yes
If yes, provide the Orphan
Designation number for this
indication:
Is this indication for a rare disease (prevalence <200,000 in U.S.)?
Does this product have an FDA
Orphan Designation for this
indication?
Yes
No
No
If yes, provide the Orphan
Designation number for this
indication:
Is this indication for a rare disease (prevalence <200,000 in U.S.)?
Does this product have an FDA
Orphan Designation for this
indication?
Yes
No
Yes
If yes, provide the Orphan
Designation number for this
indication:
Is this indication for a rare disease (prevalence <200,000 in U.S.)?
Does this product have an FDA
Orphan Designation for this
indication?
Yes
No
No
If yes, provide the Orphan
Designation number for this
indication:
Is this indication for a rare disease (prevalence <200,000 in U.S.)?
Does this product have an FDA
Orphan Designation for this
indication?
Yes
No
Yes
If yes, provide the Orphan
Designation number for this
indication:
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FIRST CONTINUATION PAGE FOR ITEM 29 – Establishment Information
Provide information for additional
establishments below, as needed.
Establishment Name
Address 1 (Street address, P.O. box, company name c/o)
Registration (FEI) Number
Address 2 (Apartment, suite, unit, building, floor, etc.)
City
MF Number
State/Province/Region
Country
ZIP or Postal Code
Is the establishment new to the application?
Yes
Establishment DUNS Number
What is the status of the establishment?
Pending
Active
No
Inactive
Withdrawn
Establishment Contact Information
Name of Contact for the Establishment
Telephone Number (Include area code)
Address 1 (Street address, P.O. box, company name c/o)
FAX Number (Include area code)
Address 2 (Apartment, suite, unit, building, floor, etc.)
City
State/Province/Region
Country
Email Address
ZIP or Postal Code
Is the site ready
Yes
for inspection?
If No, when will site be
ready? (mm/dd/yyyy)
Manufacturing Steps and/or Type of Testing
No
N/A
Establishment Name
Address 1 (Street address, P.O. box, company name c/o)
Registration (FEI) Number
Address 2 (Apartment, suite, unit, building, floor, etc.)
City
MF Number
State/Province/Region
Country
ZIP or Postal Code
Is the establishment new to the application?
Yes
Establishment DUNS Number
What is the status of the establishment?
Pending
Active
No
Inactive
Withdrawn
Establishment Contact Information
Name of Contact for the Establishment
Telephone Number (Include area code)
Address 1 (Street address, P.O. box, company name c/o)
FAX Number (Include area code)
Address 2 (Apartment, suite, unit, building, floor, etc.)
City
Country
State/Province/Region
Email Address
ZIP or Postal Code
Is the site ready
Yes
for inspection?
If No, when will site be
ready? (mm/dd/yyyy)
Manufacturing Steps and/or Type of Testing
No
N/A
Add Second Continuation Page for #29
FORM FDA 356h (1/14)
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SECOND CONTINUATION PAGE FOR ITEM 29 – Establishment Information
Provide information for additional
establishments below, as needed.
Establishment Name
Address 1 (Street address, P.O. box, company name c/o)
Registration (FEI) Number
Address 2 (Apartment, suite, unit, building, floor, etc.)
City
MF Number
State/Province/Region
Country
ZIP or Postal Code
Is the establishment new to the application?
Yes
Establishment DUNS Number
What is the status of the establishment?
Pending
Active
No
Inactive
Withdrawn
Establishment Contact Information
Name of Contact for the Establishment
Telephone Number (Include area code)
Address 1 (Street address, P.O. box, company name c/o)
FAX Number (Include area code)
Address 2 (Apartment, suite, unit, building, floor, etc.)
City
State/Province/Region
Country
Email Address
ZIP or Postal Code
Is the site ready
Yes
for inspection?
If No, when will site be
ready? (mm/dd/yyyy)
Manufacturing Steps and/or Type of Testing
No
N/A
Establishment Name
Address 1 (Street address, P.O. box, company name c/o)
Registration (FEI) Number
Address 2 (Apartment, suite, unit, building, floor, etc.)
City
MF Number
State/Province/Region
Country
ZIP or Postal Code
Is the establishment new to the application?
Yes
Establishment DUNS Number
What is the status of the establishment?
Pending
Active
No
Inactive
Withdrawn
Establishment Contact Information
Name of Contact for the Establishment
Telephone Number (Include area code)
Address 1 (Street address, P.O. box, company name c/o)
FAX Number (Include area code)
Address 2 (Apartment, suite, unit, building, floor, etc.)
City
Country
State/Province/Region
Email Address
ZIP or Postal Code
Is the site ready
Yes
for inspection?
If No, when will site be
ready? (mm/dd/yyyy)
Manufacturing Steps and/or Type of Testing
No
N/A
Add Third Continuation Page for #29
FORM FDA 356h (1/14)
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THIRD CONTINUATION PAGE FOR ITEM 29 – Establishment Information
Provide information for additional
establishments below, as needed.
Establishment Name
Address 1 (Street address, P.O. box, company name c/o)
Registration (FEI) Number
Address 2 (Apartment, suite, unit, building, floor, etc.)
City
MF Number
State/Province/Region
Country
ZIP or Postal Code
Is the establishment new to the application?
Yes
Establishment DUNS Number
What is the status of the establishment?
Pending
Active
No
Inactive
Withdrawn
Establishment Contact Information
Name of Contact for the Establishment
Telephone Number (Include area code)
Address 1 (Street address, P.O. box, company name c/o)
FAX Number (Include area code)
Address 2 (Apartment, suite, unit, building, floor, etc.)
City
State/Province/Region
Country
Email Address
ZIP or Postal Code
Is the site ready
Yes
for inspection?
If No, when will site be
ready? (mm/dd/yyyy)
Manufacturing Steps and/or Type of Testing
No
N/A
Establishment Name
Address 1 (Street address, P.O. box, company name c/o)
Registration (FEI) Number
Address 2 (Apartment, suite, unit, building, floor, etc.)
City
MF Number
State/Province/Region
Country
ZIP or Postal Code
Is the establishment new to the application?
Yes
Establishment DUNS Number
What is the status of the establishment?
Pending
Active
No
Inactive
Withdrawn
Establishment Contact Information
Name of Contact for the Establishment
Telephone Number (Include area code)
Address 1 (Street address, P.O. box, company name c/o)
FAX Number (Include area code)
Address 2 (Apartment, suite, unit, building, floor, etc.)
City
Country
State/Province/Region
Email Address
ZIP or Postal Code
Is the site ready
Yes
for inspection?
If No, when will site be
ready? (mm/dd/yyyy)
Manufacturing Steps and/or Type of Testing
No
N/A
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FOURTH CONTINUATION PAGE FOR ITEM 29 – Establishment Information
Provide information for additional
establishments below, as needed.
Establishment Name
Address 1 (Street address, P.O. box, company name c/o)
Registration (FEI) Number
Address 2 (Apartment, suite, unit, building, floor, etc.)
City
MF Number
State/Province/Region
Country
ZIP or Postal Code
Is the establishment new to the application?
Yes
Establishment DUNS Number
What is the status of the establishment?
Pending
Active
No
Inactive
Withdrawn
Establishment Contact Information
Name of Contact for the Establishment
Telephone Number (Include area code)
Address 1 (Street address, P.O. box, company name c/o)
FAX Number (Include area code)
Address 2 (Apartment, suite, unit, building, floor, etc.)
City
State/Province/Region
Country
Email Address
ZIP or Postal Code
Is the site ready
Yes
for inspection?
If No, when will site be
ready? (mm/dd/yyyy)
Manufacturing Steps and/or Type of Testing
No
N/A
Establishment Name
Address 1 (Street address, P.O. box, company name c/o)
Registration (FEI) Number
Address 2 (Apartment, suite, unit, building, floor, etc.)
City
MF Number
State/Province/Region
Country
ZIP or Postal Code
Is the establishment new to the application?
Yes
Establishment DUNS Number
What is the status of the establishment?
Pending
Active
No
Inactive
Withdrawn
Establishment Contact Information
Name of Contact for the Establishment
Telephone Number (Include area code)
Address 1 (Street address, P.O. box, company name c/o)
FAX Number (Include area code)
Address 2 (Apartment, suite, unit, building, floor, etc.)
City
Country
State/Province/Region
Email Address
ZIP or Postal Code
Is the site ready
Yes
for inspection?
If No, when will site be
ready? (mm/dd/yyyy)
Manufacturing Steps and/or Type of Testing
No
N/A
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FORM FDA 356h (1/14)
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FIFTH CONTINUATION PAGE FOR ITEM 29 – Establishment Information
Provide information for additional
establishments below, as needed.
Establishment Name
Address 1 (Street address, P.O. box, company name c/o)
Registration (FEI) Number
Address 2 (Apartment, suite, unit, building, floor, etc.)
City
MF Number
State/Province/Region
Country
ZIP or Postal Code
Is the establishment new to the application?
Yes
Establishment DUNS Number
What is the status of the establishment?
Pending
Active
No
Inactive
Withdrawn
Establishment Contact Information
Name of Contact for the Establishment
Telephone Number (Include area code)
Address 1 (Street address, P.O. box, company name c/o)
FAX Number (Include area code)
Address 2 (Apartment, suite, unit, building, floor, etc.)
City
State/Province/Region
Country
Email Address
ZIP or Postal Code
Is the site ready
Yes
for inspection?
If No, when will site be
ready? (mm/dd/yyyy)
Manufacturing Steps and/or Type of Testing
No
N/A
Establishment Name
Address 1 (Street address, P.O. box, company name c/o)
Registration (FEI) Number
Address 2 (Apartment, suite, unit, building, floor, etc.)
City
MF Number
State/Province/Region
Country
ZIP or Postal Code
Is the establishment new to the application?
Yes
Establishment DUNS Number
What is the status of the establishment?
Pending
Active
No
Inactive
Withdrawn
Establishment Contact Information
Name of Contact for the Establishment
Telephone Number (Include area code)
Address 1 (Street address, P.O. box, company name c/o)
FAX Number (Include area code)
Address 2 (Apartment, suite, unit, building, floor, etc.)
City
Country
State/Province/Region
Email Address
ZIP or Postal Code
Is the site ready
Yes
for inspection?
If No, when will site be
ready? (mm/dd/yyyy)
Manufacturing Steps and/or Type of Testing
No
N/A
Add Sixth Continuation Page for #29
FORM FDA 356h (1/14)
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SIXTH CONTINUATION PAGE FOR ITEM 29 – Establishment Information
Provide information for additional
establishments below, as needed.
Establishment Name
Address 1 (Street address, P.O. box, company name c/o)
Registration (FEI) Number
Address 2 (Apartment, suite, unit, building, floor, etc.)
City
MF Number
State/Province/Region
Country
ZIP or Postal Code
Is the establishment new to the application?
Yes
Establishment DUNS Number
What is the status of the establishment?
Pending
Active
No
Inactive
Withdrawn
Establishment Contact Information
Name of Contact for the Establishment
Telephone Number (Include area code)
Address 1 (Street address, P.O. box, company name c/o)
FAX Number (Include area code)
Address 2 (Apartment, suite, unit, building, floor, etc.)
City
State/Province/Region
Country
Email Address
ZIP or Postal Code
Is the site ready
Yes
for inspection?
If No, when will site be
ready? (mm/dd/yyyy)
Manufacturing Steps and/or Type of Testing
No
N/A
Establishment Name
Address 1 (Street address, P.O. box, company name c/o)
Registration (FEI) Number
Address 2 (Apartment, suite, unit, building, floor, etc.)
City
MF Number
State/Province/Region
Country
ZIP or Postal Code
Is the establishment new to the application?
Yes
Establishment DUNS Number
What is the status of the establishment?
Pending
Active
No
Inactive
Withdrawn
Establishment Contact Information
Name of Contact for the Establishment
Telephone Number (Include area code)
Address 1 (Street address, P.O. box, company name c/o)
FAX Number (Include area code)
Address 2 (Apartment, suite, unit, building, floor, etc.)
City
Country
State/Province/Region
Email Address
ZIP or Postal Code
Is the site ready
Yes
for inspection?
If No, when will site be
ready? (mm/dd/yyyy)
Manufacturing Steps and/or Type of Testing
No
N/A
Add Seventh Continuation Page for #29
FORM FDA 356h (1/14)
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SEVENTH CONTINUATION PAGE FOR ITEM 29 – Establishment Information
Provide information for additional
establishments below, as needed.
Establishment Name
Address 1 (Street address, P.O. box, company name c/o)
Registration (FEI) Number
Address 2 (Apartment, suite, unit, building, floor, etc.)
City
MF Number
State/Province/Region
Country
ZIP or Postal Code
Is the establishment new to the application?
Yes
Establishment DUNS Number
What is the status of the establishment?
Pending
Active
No
Inactive
Withdrawn
Establishment Contact Information
Name of Contact for the Establishment
Telephone Number (Include area code)
Address 1 (Street address, P.O. box, company name c/o)
FAX Number (Include area code)
Address 2 (Apartment, suite, unit, building, floor, etc.)
City
State/Province/Region
Country
Email Address
ZIP or Postal Code
Is the site ready
Yes
for inspection?
If No, when will site be
ready? (mm/dd/yyyy)
Manufacturing Steps and/or Type of Testing
No
N/A
Establishment Name
Address 1 (Street address, P.O. box, company name c/o)
Registration (FEI) Number
Address 2 (Apartment, suite, unit, building, floor, etc.)
City
MF Number
State/Province/Region
Country
ZIP or Postal Code
Is the establishment new to the application?
Yes
Establishment DUNS Number
What is the status of the establishment?
Pending
Active
No
Inactive
Withdrawn
Establishment Contact Information
Name of Contact for the Establishment
Telephone Number (Include area code)
Address 1 (Street address, P.O. box, company name c/o)
FAX Number (Include area code)
Address 2 (Apartment, suite, unit, building, floor, etc.)
City
Country
State/Province/Region
Email Address
ZIP or Postal Code
Is the site ready
Yes
for inspection?
If No, when will site be
ready? (mm/dd/yyyy)
Manufacturing Steps and/or Type of Testing
No
N/A
Add Eighth Continuation Page for #29
FORM FDA 356h (1/14)
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EIGHTH CONTINUATION PAGE FOR ITEM 29 – Establishment Information
Provide information for additional
establishments below, as needed.
Establishment Name
Address 1 (Street address, P.O. box, company name c/o)
Registration (FEI) Number
Address 2 (Apartment, suite, unit, building, floor, etc.)
City
MF Number
State/Province/Region
Country
ZIP or Postal Code
Is the establishment new to the application?
Yes
Establishment DUNS Number
What is the status of the establishment?
Pending
Active
No
Inactive
Withdrawn
Establishment Contact Information
Name of Contact for the Establishment
Telephone Number (Include area code)
Address 1 (Street address, P.O. box, company name c/o)
FAX Number (Include area code)
Address 2 (Apartment, suite, unit, building, floor, etc.)
City
State/Province/Region
Country
Email Address
ZIP or Postal Code
Is the site ready
Yes
for inspection?
If No, when will site be
ready? (mm/dd/yyyy)
Manufacturing Steps and/or Type of Testing
No
N/A
Establishment Name
Address 1 (Street address, P.O. box, company name c/o)
Registration (FEI) Number
Address 2 (Apartment, suite, unit, building, floor, etc.)
City
MF Number
State/Province/Region
Country
ZIP or Postal Code
Is the establishment new to the application?
Yes
Establishment DUNS Number
What is the status of the establishment?
Pending
Active
No
Inactive
Withdrawn
Establishment Contact Information
Name of Contact for the Establishment
Telephone Number (Include area code)
Address 1 (Street address, P.O. box, company name c/o)
FAX Number (Include area code)
Address 2 (Apartment, suite, unit, building, floor, etc.)
City
Country
State/Province/Region
Email Address
ZIP or Postal Code
Is the site ready
Yes
for inspection?
If No, when will site be
ready? (mm/dd/yyyy)
Manufacturing Steps and/or Type of Testing
No
N/A
Add Ninth Continuation Page for #29
FORM FDA 356h (1/14)
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NINTH CONTINUATION PAGE FOR ITEM 29 – Establishment Information
Provide information for additional
establishments below, as needed.
Establishment Name
Address 1 (Street address, P.O. box, company name c/o)
Registration (FEI) Number
Address 2 (Apartment, suite, unit, building, floor, etc.)
City
MF Number
State/Province/Region
Country
ZIP or Postal Code
Is the establishment new to the application?
Yes
Establishment DUNS Number
What is the status of the establishment?
Pending
Active
No
Inactive
Withdrawn
Establishment Contact Information
Name of Contact for the Establishment
Telephone Number (Include area code)
Address 1 (Street address, P.O. box, company name c/o)
FAX Number (Include area code)
Address 2 (Apartment, suite, unit, building, floor, etc.)
City
State/Province/Region
Country
Email Address
ZIP or Postal Code
Is the site ready
Yes
for inspection?
If No, when will site be
ready? (mm/dd/yyyy)
Manufacturing Steps and/or Type of Testing
No
N/A
Establishment Name
Address 1 (Street address, P.O. box, company name c/o)
Registration (FEI) Number
Address 2 (Apartment, suite, unit, building, floor, etc.)
City
MF Number
State/Province/Region
Country
ZIP or Postal Code
Is the establishment new to the application?
Yes
Establishment DUNS Number
What is the status of the establishment?
Pending
Active
No
Inactive
Withdrawn
Establishment Contact Information
Name of Contact for the Establishment
Telephone Number (Include area code)
Address 1 (Street address, P.O. box, company name c/o)
FAX Number (Include area code)
Address 2 (Apartment, suite, unit, building, floor, etc.)
City
Country
State/Province/Region
Email Address
ZIP or Postal Code
Is the site ready
Yes
for inspection?
If No, when will site be
ready? (mm/dd/yyyy)
Manufacturing Steps and/or Type of Testing
No
N/A
Add Tenth Continuation Page for #29
FORM FDA 356h (1/14)
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TENTH CONTINUATION PAGE FOR ITEM 29 – Establishment Information
Provide information for additional
establishments below, as needed.
Establishment Name
Address 1 (Street address, P.O. box, company name c/o)
Registration (FEI) Number
Address 2 (Apartment, suite, unit, building, floor, etc.)
City
MF Number
State/Province/Region
Country
ZIP or Postal Code
Is the establishment new to the application?
Yes
Establishment DUNS Number
What is the status of the establishment?
Pending
Active
No
Inactive
Withdrawn
Establishment Contact Information
Name of Contact for the Establishment
Telephone Number (Include area code)
Address 1 (Street address, P.O. box, company name c/o)
FAX Number (Include area code)
Address 2 (Apartment, suite, unit, building, floor, etc.)
City
State/Province/Region
Country
Email Address
ZIP or Postal Code
Is the site ready
Yes
for inspection?
If No, when will site be
ready? (mm/dd/yyyy)
Manufacturing Steps and/or Type of Testing
No
N/A
Establishment Name
Address 1 (Street address, P.O. box, company name c/o)
Registration (FEI) Number
Address 2 (Apartment, suite, unit, building, floor, etc.)
City
MF Number
State/Province/Region
Country
ZIP or Postal Code
Is the establishment new to the application?
Yes
Establishment DUNS Number
What is the status of the establishment?
Pending
Active
No
Inactive
Withdrawn
Establishment Contact Information
Name of Contact for the Establishment
Telephone Number (Include area code)
Address 1 (Street address, P.O. box, company name c/o)
FAX Number (Include area code)
Address 2 (Apartment, suite, unit, building, floor, etc.)
City
Country
State/Province/Region
ZIP or Postal Code
Is the site ready
Yes
for inspection?
If No, when will site be
ready? (mm/dd/yyyy)
Manufacturing Steps and/or Type of Testing
FORM FDA 356h (1/14)
Email Address
Page X of X
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No
N/A
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CONTINUATION PAGE FOR ITEM 30 – Cross References
Continue your answer in the space below.
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FORM FDA 356h (1/14)
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File Type | application/pdf |
File Title | FDA-356h_clean.indd |
Author | PSC Publishing Services |
File Modified | 2014-02-26 |
File Created | 2014-02-11 |