21 CFR 1321.01 - DEA mailing addresses.

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§ 1321.01 DEA mailing addresses.

The following table provides information regarding mailing addresses to be used when sending specified correspondence to the Drug Enforcement Administration.

Table of DEA Mailing Addresses

Code of Federal Regulations Section - Topic DEA mailing address
DEA Administrator
1308.43(b) - Petition to initiate proceedings for rulemaking.
1316.23(b) - Petition for grant of confidentiality for research subjects.
1316.24(b) - Petition for exemption from prosecution for researchers.
Drug Enforcement Administration, Attn: Administrator, 8701 Morrissette Drive, Springfield, VA 22152.
DEA Diversion Control Division
1307.03 - Exception request filing.
1307.22 - Delivery of surrendered and forfeited controlled substances.
1310.21(b) - Sale by Federal departments or agencies of chemicals which could be used to manufacture controlled substances certification request. 2
Drug Enforcement Administration, Attn: Diversion Control Division/DC, 8701 Morrissette Drive, Springfield, VA 22152.
DEA Regulatory Section
1301.71(d) - Security system compliance review for controlled substances.
1309.71(c) - Security system compliance review for List I chemicals.
1310.03(c) - Mail-Order reports involving transactions with nonregulated persons or exports. 1
1310.05(b)(1) - Unusual or excessive loss or disappearance of listed chemicals.
1310.05(b)(2) - Reports of domestic regulated transactions in a tableting machine or an encapsulating machine. 1
1310.05(c)(1) - Reports of imports and exports of a tableting machine or an encapsulating machine. 1
1310.05(c)(2) - Report of declared exports of machines refused, rejected, or returned.
1312.12(a) - Application for import permit (DEA Form 357). 1
1312.18(b) - Import declaration (DEA Form 236) submission. 1
1312.22(g)(8) - Request for return of unacceptable or undeliverable exported controlled substances. 1
1312.27(a) - Controlled substances export declaration (DEA Form 236) filing. 1
1312.31(b) - Controlled substances transshipment permit application.
1312.32(a) - Advanced notice of importation for transshipment or transfer of controlled substances.
1313.12(b) - Authorization to import listed chemicals (DEA Form 486/486A). 1
1313.12(e) - Quarterly reports of listed chemicals importation.
1313.21(b) - Authorization to export listed chemicals (DEA Form 486). 1
1313.21(e) - Quarterly reports of listed chemicals exportation.
1313.22(c) - Notice of declared exports of listed chemicals refused, rejected or undeliverable. 1
1313.31(b) - Advanced notice of importation for transshipment or transfer of listed chemicals.
1313.32(b)(1) - International transaction authorization (DEA Form 486). 1
1314.110(a)(1) - Reports for mail-order sales.
1314.110(a)(2) - Request to submit mail-order sales reports.
Drug Enforcement Administration, Attn: Regulatory Section/DRG, 8701 Morrissette Drive, Springfield, VA 22152.
DEA Drug & Chemical Evaluation Section
1308.21(a) - Exclusion of nonnarcotic substance.
1308.23(b) - Exemption for chemical preparations.
1308.24(d) - Exempt narcotic chemical preparations importer/exporter reporting.
1308.24(i) - Exempted chemical preparations listing.
1308.25(a) - Exclusion of veterinary anabolic steroid implant product application.
1308.26(a) - Excluded veterinary anabolic steroid implant products listing.
1308.31(a) - Exemption of a nonnarcotic prescription product application.
1308.32 - Exempted prescription products listing.
1308.33(b) - Exemption of certain anabolic steroid products application.
1308.34 - Exempted anabolic steroid products listing.
1310.13(b) - Exemption for chemical preparations.
1310.05(d) - Bulk manufacturer of listed chemicals reporting.
Drug Enforcement Administration, Attn: Drug & Chemical Evaluation Section/DRE, 8701 Morrissette Drive, Springfield, VA 22152.
UN Reporting & Quota Section
1303.12(b) - Application for controlled substances procurement quota (DEA Form 250) filing and request. Drug Enforcement Administration, Attn: UN Reporting & Quota Section/DRQ, 8701 Morrissette Drive, Springfield, VA 22152.
1303.12(d) - Controlled substances quota adjustment request.
1303.22 - Application for individual manufacturing quota (DEA Form 189) filing and request for schedule I or II controlled substances.
1304.31(a) - Manufacturers importing narcotic raw material report submission.
1304.32(a) - Manufacturers importing coca leaves report submission.
1315.22 - Application for individual manufacturing quota for ephedrine, pseudoephedrine, phenylpropanolamine (DEA Form 189) filing and request.
1315.32(e) - Application for procurement quota for ephedrine, pseudoephedrine, phenylpropanolamine (DEA Form 250) filing and request.
1315.32(g) - Procurement quota adjustment request for ephedrine, pseudoephedrine, and phenylpropanolamine.
1315.34(d) - Application for import quota for ephedrine, pseudoephedrine, phenylpropanolamine (DEA Form 488) request and filing.
1315.36(b) - Request import quota increase for ephedrine, pseudoephedrine, or phenylpropanolamine.
Pharmaceutical Investigations Section
1304.04(d) - ARCOS separate central reporting identifier request.
1304.33(a) - Reports to ARCOS.
Drug Enforcement Administration, Attn: ARCOS Unit/DOPT, P.O. Box 2520, Springfield, VA 22152-2520 OR Drug Enforcement Administration, Attn: ARCOS Unit, 8701 Morrissette Drive, Springfield, VA 22152.
DEA Registration Section
1301.03 - Procedures information request (controlled substances registration).
1301.13(e)(2) - Request DEA Forms 224, 225, and 363.
1301.14(a) - Controlled substances registration application submission.
1301.18(c) - Research project controlled substance increase request.
1301.51 - Controlled substances registration modification request.
1301.52(b) - Controlled substances registration transfer request.
1301.52(c) - Controlled substances registration discontinuance of business activities notification.
1309.03 - List I chemicals registration procedures information request.
1309.32(c) - Request DEA Form 510.
1309.33(a) - List I chemicals registration application submission.
1309.61 - List I chemicals registration modification request.
Drug Enforcement Administration, Attn: Registration Section/DRR P.O. Box 2639, Springfield, VA 22152-2639.
DEA Hearing Clerk
1301.43 - Request for hearing or appearance; waiver.
1303.34 - Request for hearing or appearance; waiver.
1308.44 - Request for hearing or appearance; waiver.
1316.45 - Hearings documentation filing.
1316.46(a) - Inspection of record.
1316.47(a) - Request for hearing.
1316.48 - Notice of appearance.
Drug Enforcement Administration, Attn: Hearing Clerk/OALJ, 8701 Morrissette Drive, Springfield, VA 22152.
DEA Federal Register Representative
1301.33(a) - Filing of written comments regarding application for bulk manufacture of Schedule I and II substances. 2
1301.34(a) - Filing of written comments regarding application for importation of Schedule I and II substances. 2
1303.11(c) - Filing of written comments regarding notice of an aggregate production quota. 2
1303.13(c) - Filing of written comments regarding adjustments of aggregate production quotas. 2
1303.13(c) - Filing of written comments regarding adjustments of aggregate production quotas. 2
1308.43(g) - Filing of written comments regarding initiation of proceedings for rulemaking. 2
Drug Enforcement Administration, Attn: Federal Register Representative/DRW, 8701 Morrissette Drive, Springfield, VA 22152.
http://www.regulations.gov/.

1 Applications/filings/reports are required to be filed electronically in accordance with this chapter.

2 Applications/filings/reports may be filed electronically in accordance with this chapter.

[81 97041, Dec. 30, 2016]

This is a list of United States Code sections, Statutes at Large, Public Laws, and Presidential Documents, which provide rulemaking authority for this CFR Part.

This list is taken from the Parallel Table of Authorities and Rules provided by GPO [Government Printing Office].

It is not guaranteed to be accurate or up-to-date, though we do refresh the database weekly. More limitations on accuracy are described at the GPO site.


United States Code
U.S. Code: Title 21 - FOOD AND DRUGS

Title 21 published on 10-May-2017 03:43

The following are ALL rules, proposed rules, and notices (chronologically) published in the Federal Register relating to 21 CFR Part 1321 after this date.

  • 2017-01-30; vol. 82 # 18 - Monday, January 30, 2017
    1. 82 FR 8688 - Revision of Import and Export Requirements for Controlled Substances, Listed Chemicals, and Tableting and Encapsulating Machines, Including Changes To Implement the International Trade Data System (ITDS); Revision of Reporting Requirements for Domestic Transactions in Listed Chemicals and Tableting and Encapsulating Machines; and Technical Amendments
      GPO FDSys XML | Text
      DEPARTMENT OF JUSTICE, Drug Enforcement Administration
      Final rule; delay of effective date.
      Effective Dates: This Final Rule is effective January 30, 2017. The effective date of the Final Rule amending 21 CFR parts 1300, 1301, 1302, 1303, 1304, 1308, 1309, 1310, 1312, 1313, 1314, 1315, 1316, and 1321 published in the Federal Register December 30, 2016, at 81 FR 96992 is delayed to March 21, 2017. However, compliance with the revisions to DEA regulations made by this rule is not required until July 31, 2017.
      21 CFR Parts 1300, 1301, 1302, 1303, 1304, 1308, 1309, 1310, 1312, 1313, 1314, 1315, 1316, and 1321
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