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.
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11. CONSENT TO RELEASE IDENTIFYING INFORMATION TO
SAMHSA BUPRENORPHINE Physician and Treatment Provider Locator WEB SITE (Read instruction 11 below before
answering)
I consent to the release of my name,
primary address, and phone number to the SAMHSA Buprenorphine Physician and Treatment Provider 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 Provider Locator Web site.
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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.)
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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)
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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.
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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.
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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).
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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.)
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11. The SAMHSA Buprenorphine Physician and Treatment Provider 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 Provider Locator Web site will be made without the express
consent of the physician.
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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
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