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pdfForm Approved: 0930-0234
Expiration Date: 05/31/2012
See OMB Statement on Reverse
Notification of Intent to Use Schedule III, IV, or V Opioid Drugs
for the Maintenance and Detoxification Treatment
of Opiate Addiction under 21 USC § 823(g)(2)
DATE OF SUBMISSION
Note: Notification is required by § 303(g)(2), Controlled Substances Act (21 USC § 823(g)(2)). See instructions on reverse. For
second notifications,
you must complete items 6, 8, 9, 10, and sign and date the form (item 12).
1a. NAME OF PRACTITIONER
b. State Medical License Number
c. DEA Registration Number
2. ADDRESS OF PRIMARY LOCATION (Include Zip Code) (See instruction
below)
3. TELEPHONE NUMBER (Include Area Code)
4. FAX NUMBER (Include Area Code)
5. EMAIL ADDRESS (Optional)
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
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 meet at least one of the following criteria and am therefore a qualifying physician (Check and provide copies of documentation for all that apply):
Subspecialty board certification in addiction psychiatry from the American Board of Medical Specialties
Addiction certification from the American Society of Addiction Medicine
Subspecialty board certification in addiction medicine from the American Osteopathic Association
Completion of not less than eight hours of training for the treatment and management of opioid-dependent patients provided by the
following organization(s):
Date and location of training
American Society of Addiction Medicine
_______________________
American Academy of Addiction Psychiatry
_____________________
American Medical Association
_______________________
American Osteopathic Association
_______________________
American Psychiatric Association
_______________________
Other (Specify, include date and location)
_______________________
Participation as an investigator in one or more clinical trials leading to the approval of a Schedule III, IV, or V narcotic drug for maintenance or
detoxification treatment
State medical licensing board-approved experience or training in the treatment and management of opioid-dependent patients
OTHER (Specify)_______________________
For
Second Notifications - I certified qualifications in my initial notification and these qualifications have not changed.
9. CERTIFICATION OF CAPACITY
I certify that I have the capacity to refer patients for appropriate counseling and other appropriate ancillary services.
10. CERTIFICATION OF MAXIMUM PATIENT LOAD
I certify that I will not exceed 30 patients for maintenance or detoxification treatment at one time.
Second Notification - I need to treat up to 100 patients and I certify that I will not exceed 100 patients for maintenance or detoxification treatment at one
time.
SMA-167
11. CONSENT TO RELEASE IDENTIFYING INFORMATION TO SAMHSA BUPRENORPHINE PHYSICIAN AND TREATMENT PROGRAM
LOCATOR WEB SITE (Read instruction 11 below before answering)
Page 2
I consent to the release of my name, primary address, and phone number to the SAMHSA Buprenorphine Physician and Treatment Program Locator Web
site.
I do not consent to the release of my name, primary address, and phone number to the SAMHSA Buprenorphine Physician and Treatment Program
Locator Web site.
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.)
__________________________________
Signature
________________
Date
Please send the completed form to:
Substance Abuse and Mental Health Services Administration
Division of Pharmacologic Therapies
Attention: Opioid Treatment Waiver Program
One Choke Cherry Road, Rm 2-1063
Rockville, MD 20857
Fax 240-276-1630
Phone 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)). 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.
2. Only one address should be specified. For the practitioner to dispense the
1. The practitioner must identify the DEA registration number issued under
narcotic drugs or combinations to be used under this notification, the primary
21 USC § 823(f) to prescribe substances controlled in Schedules III, IV, or V.
address listed here must be the same primary address listed in the
practitioner’s registration under § 823(f).
6. 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.
Second Notification - For physicians who submitted a new notification not less than one year ago and intend and need to treat up to 100 patients. (See Office of
National Drug Control Policy Reauthorization Act of 2006.)
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 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); Room 71-1044, One Choke Cherry Road, Rockville,
MD 20857
File Type | application/pdf |
File Title | Notification of Intent to Use Schedule III, IV, or V Opioid Drugs for the Maintenance and Detoxification Treatment of Opiate Add |
Author | Center for Substance Abuse Treatment |
File Modified | 2010-10-22 |
File Created | 2006-12-15 |