Form NOI Form NOI Form NOI Form

Notification of Intent to Use Schedule III, IV, or V Opioid Drugs for the Maintenance and Detoxification Treatment of Opiate Addiction by a “Qualifying Other Practitioner” under 21 USC  § 823(g)(2) To Complete Online Go To: http://buprenorphine.samhsa.gov/pls/bwns/waiver	Form Approved: XXXX-XXXX Date: XX/XX/XXXX See OMB Statement Below
	DATE OF SUBMISSION
Note:  Notification is required by § 303(g)(2), Controlled Substances Act (21 USC § 823(g)(2)). See instructions on reverse. PLEASE DON’T FORGET TO SIGN AND DATE THIS FORM (ITEM 9)
1A. NAME OF PRACTITIONER 1B. State Health Professional License Number 1C. Professional Discipline 1D. DEA Registration Number
2. ADDRESS OF PRACTICE LOCATION (Include Zip Code) (See instruction below) 2A. Is this location a FQHC? Yes No	3. TELEPHONE NUMBER (Include Area Code) 4. FAX NUMBER (Include Area Code) 5. EMAIL ADDRESS (Required)
6. PURPOSE OF NOTIFICATION (See instruction below) New Notification New Notification, with the intent to immediately facilitate treatment of an individual (one) patient Second notification of need and intent to treat up to 100 patients
7. CERTIFICATION OF USE OF NARCOTIC DRUGS UNDER THIS NOTIFICATION When providing maintenance or detoxification treatment, I certify that I will only use Schedule III, IV, or V drugs or combinations of drugs that have been approved by the FDA for use in maintenance or detoxification treatment and that have not been the subject of an adverse determination.
8. Certification of Qualifying Criteria I certify that I am either an advanced practice nurse or physician assistant who satisfies the definition of a “qualifying other practitioner” under 21 U.S.C. § 823(g)(2)(G)(iv), as amended by the Comprehensive Addiction and Recovery Act of 2016, and that I am aware that ‘qualifying other practitioners’ will be included in the definition of a “qualifying practitioner” under 21 U.S.C. § 823(g)(2)(G)(iii) until October 1, 2021. I certify that I am licensed to prescribe Schedule III, IV, or V medications for the treatment of pain under State law. (To verify Mid-Level Practitioners Authorization by State please visit https://www.deadiversion.usdoj.gov/drugreg/practioners/mlp_by_state.pdf.) I certify that I am NOT required by State law to be supervised by and work in collaboration with a qualifying physician to prescribe Schedule III, IV, or V medications. or I certify that I am required by State law to be supervised by and work in collaboration with a qualifying physician to prescribe III, IV, or V medications. Supervisory Physician Name: _______________________________________ Supervisory Physician Phone Number: ________________________________ I certify that I have completed the required 24 hours of training for the treatment and management of opioid-dependent patients and am therefore a qualifying other practitioner. Name of organization approved for training: _________________________________________________________________________ Please Provide Date of Completion: _______________________________________________________________________________
9. Certification of Capacity I certify that I have the capacity to provide patients with appropriate counseling and other appropriate ancillary services, either directly or by referral. I certify that I have the capacity to all drugs approved by the Food and Drug Administration for the treatment of opioid use disorder, including for maintenance, detoxification, overdose reversal, and relapse prevention.
10. Certification of Maximum Patient Load (select one) I certify that I will not exceed 30 patients for maintenance or detoxification treatment at one time.
11. CONSENT (Read instruction 11 below before answering) I consent to the release of my name, primary address, and phone number to the SAMHSA Treatment Locators. I do not consent to the release of my name, primary address, and phone number to the SAMHSA Treatment Locators.
12. I certify that the information presented above is true and correct to the best of my knowledge. I certify that I will notify SAMHSA at the address below if any of the information contained on this form changes. Note: Any false, fictitious, or fraudulent statements or information presented above or misrepresentations relative thereto may violate Federal laws and could subject you to prosecution, and/or monetary penalties, and or denial, revocation, or suspension of DEA registration. (See 18 USC § 1001; 31 USC §§ 3801–3812; 21 USC § 824.)  X__________________________________  X ________________________ Signature Date

Substance Abuse and Mental Health Services Administration, Division of Pharmacologic Therapies Please submit form electronically to: http://buprenorphine.samhsa.gov/pls/bwns/waiver For questions, please call 1-866-287-2728 (1-866-BUP-CSAT)	This form is intended to facilitate the implementation of the provisions of 21 USC  § 823(g)(2). The Secretary of DHHS will use the information provided to determine whether practitioners meet the qualifications for waivers from the separate registration requirements under the Controlled Substances Act (21 USC  § 823(g)(1)). If such qualifications are met, the Drug Enforcement Administration will assign an identification number to qualifying practitioners and the number will be included in the practitioner’s registration under 21 USC § 823(f).This form may be completed and submitted electronically (including facsimile) to facilitate processing.
1. The practitioner must identify the DEA registration number issued under 21 USC § 823(f) to prescribe substances controlled in Schedules III, IV, or V.	2. Only one address should be specified. For the practitioner to dispense the narcotic drugs or combinations to be used under this notification, the primary address listed here must be the same primary address listed in the practitioner's registration under § 823(f).
7. Purpose of notification: New Notification - an initial notification for a waiver submitted for the purpose of obtaining an identification number from DEA for inclusion in the registration under 21 USC § 823(f).  New Notification, with the intent to immediately facilitate treatment of an individual (one) patient - an initial notification submitted for the purpose described above, with the additional purpose of notifying the Secretary and the Attorney General of the intent to provide immediate opiate addiction treatment for an individual (one) patient pending processing of this waiver notification. Increase to 100 Notification - For physicians who submitted a new notification not less than one year ago and intend and need to treat up to 100 patients.
11. The SAMHSA Buprenorphine Physician and Treatment Program Locator Web site is publicly accessible at http://buprenorphine.samhsa.gov/bwns_locator/. The Locator Web site lists the names and practice contact information of physicians with DATA waivers, which allow them to treat opioid addiction with Schedule III, IV, and V opioid medications, who agree to be listed on the site. The Locator Web site is used by the treatment-seeking public and health care professionals to find physicians with DATA waivers. The Locator Web site additionally provides links to many other sources of information on substance abuse. No physician listings on the SAMHSA Buprenorphine Physician and Treatment Program Locator Web site will be made without the express consent of the physician.
Privacy Act Information Authority: Section 303 of the Controlled Substances Act of 1970 (21 USC § 823(g)(2)). Purpose: To obtain information required to determine whether a practitioner meets the requirements of 21 USC § 823(g)(2).Routine Uses: Disclosures of information from this system are made to the following categories of users for the purposes stated: A. Medical specialty societies to verify practitioner qualifications. B. Other federal law enforcement and regulatory agencies for law enforcement and regulatory purposes. C. State and local law enforcement and regulatory agencies for law enforcement and regulatory purposes. D. Persons registered under the Controlled Substance Act (PL 91-513) for the purpose of verifying the registration of customers and practitioners. Effect: This form was created to facilitate the submission and review of waivers under 21 USC § 823(g)(2). This does not preclude other forms of notification.		Paperwork Reduction Act Statement Public reporting burden for completing this form is estimated to average 4 minutes per response, including the time for reviewing instructions, searching existing data sources, gathering and maintaining the data needed, and completing and reviewing the completed form. 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 project is 0930-0234. Send comments regarding this burden estimate or any other aspect of this collection of information, including suggestions for reducing this burden, to SAMHSA Reports Clearance Officer; Paperwork Reduction Project (0930-0234); 5600 Fishers Lane, Rockville, MD 20857

REVISED: 11/29/16