Documents

Schedules of Controlled Substances: Placement of Lacosamide into Schedule V

Federal Register · Rule · May 21, 2009

Comments Received DEA received one comment within the comment period in response to the Notice of Proposed Rulemaking. … DEA also received many comments after the comment period closed. These late comments were not considered by DEA.

Controlled Substances: Proposed Aggregate Production Quotas for 2011

Federal Register · Notice · Sep 15, 2010

Please note that DEA is requesting that electronic comments be submitted before midnight Eastern Time on the day the comment period closes. … Please note that the Freedom of Information Act applies to all comments received.

Technical Amendment to Listing in Schedule III of Approved Drug Products Containing Tetrahydrocannabinols; Withdrawal of Proposed Rule

Federal Register · Proposed Rule · Sep 29, 2008

During the comment period, DEA received comments from nine entities (firms, organizations, and one individual). … DEA believes the former approach, as compared to the latter, is most likely to result in such rescheduling becoming effective in the shortest period of time. Dated: September 18, 2008.

Controlled Substances: Established Initial Aggregate Production Quotas for 2000

Federal Register · Notice · Dec 28, 1999

Six companies commented on a total of 16 Schedules I and II controlled substances within the published comment period. … In addition, one comment was received after the published comment period had ended.

Information on Foreign Chain of Distribution for Ephedrine, Pseudoephedrine, and Phenylpropanolamine

Federal Register · Rule · Mar 5, 2010

Imports handled by the foreign distributor may not be restricted during the 60-day period. … DEA solicited comments regarding the Paperwork Reduction Act aspects of the Notice of Proposed Rulemaking and received no comments.

Clarification Regarding the Supplier's DEA Registration Number on the Single-Sheet DEA Form 222

Federal Register · Rule · Jul 20, 2021

Commenters should be aware that the electronic Federal Docket Management System will not accept comments after 11:59 p.m. Eastern Time on the last day of the comment period. … Regulatory Flexibility Act The Regulatory Flexibility Act (RFA) (5 U.S.C. 601-612) applies to rules that are subject to notice and comment under section 553(b) of the APA or other laws.

Reexportation of Controlled Substances

Federal Register · Rule · Dec 26, 2007

Comments Received DEA received nine comments on the Notice of Proposed Rulemaking. … DEA received one comment discussing this issue. The commenter supported DEA's position, agreeing that such an interpretation was contemplated in the Controlled Substances Export Reform Act.

Townwood Pharmacy; Revocation of Registration

Federal Register · Notice · Feb 19, 1998

The audit covered the period February 26, 1993 to January 25, 1994, and revealed discrepancies for nine of the audited substances. … For less than a one year period of time, Respondent could not account for over 13,500 dosage units of controlled substances.

Implementation of the Comprehensive Methamphetamine Control Act of 1996; Regulation of Pseudoephedrine, Phenylpropanolamine, and Combination Ephedrine Drug Products and Reports of Certain Transactions to Nonregulated Persons

Federal Register · Rule · Mar 28, 2002

What Comments Were Received? The comment period for the NPRM closed on December 8, 1997. … Further, the MCA reduced the record retention period from 4 years to 2 years.

Schedules of Controlled Substances: Placement of Methylone Into Schedule I

Federal Register · Rule · Apr 12, 2013

Act and the Controlled Substances Import and Export Act (21 U.S.C. 801-971), as amended (hereinafter, “CSA”). … Congressional Review Act This rule is not a major rule as defined by § 804 of the Small Business Regulatory Enforcement Fairness Act of 1996 (Congressional Review Act (CRA)).

Established Assessment of Annual Needs for the List I Chemicals Ephedrine, Pseudoephedrine, and Phenylpropanolamine for 2009

Federal Register · Notice · Jul 9, 2009

All comments received during the comment period are discussed further below. … This action is not a major rule as defined by Section 804 of the Small Business Regulatory Enforcement Fairness Act of 1996 (Congressional Review Act).

Expansion of Induction of Buprenorphine via Telemedicine Encounter

Federal Register · Proposed Rule · Mar 1, 2023

Commenters should be aware that the electronic Federal Docket Management System will not accept comments after 11:59 p.m. Eastern Time on the last day of the comment period. … The Freedom of Information Act applies to all comments received.

Ordering Schedule I and II Controlled Substances Using DEA Form 222; Technical Amendments

Federal Register · Rule · Mar 20, 2026

During the comment period, DEA received numerous comments about the POAs, noting that the proposed amendment would be more restrictive than the then-current rule with respect to who could sign a POA. … Regulatory Flexibility Act The Regulatory Flexibility Act (RFA) (5 U.S.C. 601-612) applies to rules that are subject to notice and comment under section 553(b) of the APA.

Agency Information Collection Activities: Proposed Collection; Comment Request

Federal Register · Notice · May 17, 2001

This proposed information collection was previously published in the Federal Register on March 13, 2001, Volume 66, Number 49, pages 14595-14596 allowing for a 60-day public comment period. … No comments were received during the 60-day comment period. The purpose of this notice is to allow an additional 30 days for public comment until June 18, 2001.

Controlled Substances: Established Initial Aggregate Production Quotas for 2001

Federal Register · Notice · Dec 19, 2000

Five companies commented on a total of twenty Schedules I and II controlled substances within the published comment period. … In addition, two comments were received after the published comment period had ended (dated November 6, 2000 and November 10, 2000).

Agency Information Collection Activities: Proposed Collection; Comments Requested; Reporting and Recordkeeping for Digital Certificates

Federal Register · Notice · Jan 8, 2010

Enforcement Administration (DEA) will be submitting the following information collection request to the Office of Management and Budget (OMB) for review and approval in accordance with the Paperwork Reduction Act … This proposed information collection was previously published in the Federal Register at 74 FR 53760 (October 20, 2009), allowing for a 60 day comment period.

Agency Information Collection Activities; Proposed Collection; Comments Requested: Reporting and Recordkeeping for Digital Certificates

Federal Register · Notice · Mar 15, 2013

Enforcement Administration (DEA) will be submitting the following information collection request to the Office of Management and Budget (OMB) for review and approval in accordance with the Paperwork Reduction Act … This proposed information collection was previously published in the Federal Register, Volume 78, Number 8, page 2442, on January 11, 2013, allowing for a 60-day comment period.

Removal of Thresholds for the List I Chemicals Pseudoephedrine and Phenylpropanolamine

Federal Register · Rule · Jul 7, 2010

The comment period for the NPRM closed on January 22, 2008. DEA received one comment on the NPRM. … DEA did not receive any comments regarding the Paperwork Reduction Act aspects of the Notice of Proposed Rulemaking.

JM Pharmacy Group, Inc., d/b/a Farmacia Nueva and Best Pharma Corp; Decision and Order

Federal Register · Notice · May 19, 2015

If the dismissal of indictment really cleaned up all issues surrounding Moro-Perez and his pharmacies, why would there even need to be a subsequent surrender of Farmacia Nueva's COR? … From Antoine's testimony, it appears that, from the period of January 31, 2009 to November 30, 2011, Dr.

Additions to Listing of Exempt Chemical Mixtures

Federal Register · Rule · Jan 27, 2020

Commenters should be aware that the electronic Federal Docket Management System will not accept comments after 11:59 p.m. Eastern Time on the last day of the comment period. … Title 21 CFR 1310.13 further specifies that within a reasonable period of time after the receipt of an application for an exemption, the Acting Administrator will notify the applicant of acceptance or