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Title: | Diversion Control Division | DEA Form 161R |
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Keywords: | Diversion Control Division |
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Body: | DEA.Registration.Help@dea.gov
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DEA Form 161R
Home
Reporting
Import/Export Permit Applications and Declarations
DEA Form 161R
Only those persons registered with and authorized by DEA to import or
export controlled substances may utilize/submit declarations and
applications for permits.
DEA Form 161R - Application for Permit to Export Controlled Substances for
Subsequent Reexport (PDF)
Instructions PDF
INFORMATION AND INSTRUCTIONS, DEA FORM 161R
This application must be completed in triplicate. The original is sent to
DEA HQs: Drug Enforcement Administration, Diversion Control Division,
Import/Export Unit, 8701 Morrissette Drive, Springfield, VA 22152. See
Instructions 5a and 9 for copies two and three.
(1) The name and address of the consignee as shown on this application and
on the permit to export must correspond with that shown on the foreign
import certificate.
(2) To avoid delays in clearance at the port of export, be sure to enter
the correct port on this application. A copy of your export permit is sent
directly to the District Director of Customs at the port indicated on the
application for comparison with the permit presented for clearance of the
shipment. The shipment will not clear at any other port without an
amendment of the permit indicating a change to that effect.
(3) The original or an authentic signed and/or notarized copy of the
foreign import certificate must accompany this application. If this
certificate is in a foreign language, a translation must accompany the
application. If this certificate is needed to accomplish entry of the drug
into the country of destination, your request for its return to you should
accompany the application.
(4) Application should be made in the name of the registered legal entity,
as shown on the DEA registration certificate, and signed by a responsible
authorized official if a corporation, by a partner, or by the person
registered as an individual. Only persons registered to export may be
issued export permits. The registrations of manufacturers, distributors,
practitioners, researchers, etc. do not entitle them to export controlled
substances.
(5) Controlled substances in Schedule I or II, or a narcotic drug in
Schedule III or IV may be exported from the United States to a country for
subsequent export from that country to another country:
a. Thirty days from the date of exportation from the United States to the
first country, the exporter must return Copy 2 of Form DEA 161R with 7c
completed, that is, with the actual date of export and actual quantity
shipped.
b. The controlled substances must be exported from the first country to the
second country no later than 180 days from the date of exportation from the
United States
c. Within 30 days after the controlled substance is exported from the first
country to the second country or the order is canceled by the second
country, the person who exported the controlled substance from the United
States must deliver to DEA Headquarters documentation certifying that such
export from the first country to the second country has occurred or was
refused.
i. The company must provide on company letterhead signed by a responsible
company official the following information: (1) Name of the second country,
(2) actual quantity shipped, (3) actual date shipped, and (4) DEA export
permit number for the original export to the first country.
ii. For refused shipments, the company must file a written request with DEA
for return, a brief summary of the facts warranting the return, and a DEA
Form 357, Application for Import Permit. DEA will evaluate the request and
return a response in writing.
(6) Permits will be mailed to the exporter at the address shown at the
bottom of the application unless contrary instructions are attached to and
made a part of this application.
(7) Identification of drugs to be exported and the controlled substance
content should be entered on the application in the following manner:
8a. NAME AND QUANTITY OF DRUG OR
PREPARATIONS TO BE EXPORTED 8b. CONTROLLED SUBSTANCE CONTENT OF
DRUG OR PREPARATION TO BE EXPORTED
(expressed as acid, base or alkaloid, not salt)
3 bottles x 100 Secobarbital Sodium capsules (100
mg/capsule) Secobarbital 24.47 gm
2 boxes x 100 Meperidine HCL ampules (5%, 2ml
ampules) Meperidine 17.43 gm
1 box x 100 Meperidine HCl vials (10%, 20 ml, vials) Meperidine 174.30 gm
2 x 1 pt. Meperidine HCL Syrup (50 mg/5ml, pints) Meperidine 8.24 gm
1 box x 100 gm Dextroamphetamine Sulfate powder Dextroamphetamine 73.38 gm.
1 bottle x 500 Hydromorphone HCl tablets (4
mg/tablets) Hydromorphone 1.77 gm
(9) Copy 3 of the Application for Permit to Export Controlled Substances
for Subsequent Reexport (Form DEA 161R) is retained by the registrant.
PRIVACY ACT INFORMATION
AUTHORITY: Section 1003 of the Controlled Substances Act of 1970 (PL-513)
PURPOSE: Control exportation of certain Controlled Substances from the
United States.
ROUTINE USES: The Controlled Substances Act Registration Records produces
special reports as required for statistical analytical purposes.
Disclosures of information from this system are made to the following
categories of users for the purposed states:
A. Other Federal law enforcement and regulatory agencies for law
enforcement and regulatory purposes.
B. State and local law enforcement and regulatory agencies for law
enforcement and regulatory purposes.
C. Persons registered under the Controlled Substances Act (Public Law
91-513).
EFFECT: No permit will be issued.
According to the Paperwork Reduction Act of 1995, no persons are required
to respond to a Collection of Information unless it displays a valid OMB
control number. The valid OMB control number for this Information
Collection is 1117-0004.
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DIVERSION CONTROL DIVISION
U.S. Department of Justice
Drug Enforcement Administration
DIVERSION CONTROL DIVISION
8701 Morrissette Drive
Springfield, VA 22152
1.800.882.9539
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