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DEA Federal Register Entry
U.S. Federal register
Date="06/29/93" Citation="58 FR 34707" Group="legal" Type="RULE" Department="DEPARTMENT OF JUSTICE" Agency="DRUG ENFORCEMENT ADMINISTRATION, DEPARTMENT OF JUSTICE" Subject="Schedules of Controlled Substances: Exempt Anabolic Steroid Products"
DEPARTMENT OF JUSTICE Drug Enforcement Administration 21 CFR Part 1308 Schedules of Controlled Substances: Exempt Anabolic Steroid Products AGENCY: Drug Enforcement Administration, Department of Justice. ACTION: Interim rule and request for comments.
DEPARTMENT OF JUSTICE Drug Enforcement Administration 21 CFR Part 1308 Schedules of Controlled Substances: Exempt Anabolic Steroid Products AGENCY: Drug Enforcement Administration, Department of Justice. ACTION: Interim rule and request for comments. + ------------------------------------------------------------ SUMMARY: The Drug Enforcement Administration (DEA) is designating two preparations as exempt anabolic steroid products. This action, as part of the ongoing implementation of the Anabolic Steroid Control Act of 1990, removes certain regulatory controls pertaining to Schedule III substances from the designated entities. DATES: Effective Date: June 29, 1993. Comments must be submitted on or before August 30, 1993. ADDRESSES: Comments and objections should be submitted to the Director, Office of Diversion Control, Drug Enforcement Administration, Washington, DC 20537; Attention: DEA Federal Register Representative/CCR. FOR FURTHER INFORMATION CONTACT: Howard McClain, Jr., (Chief, Drug and Chemical Evaluation Section), 202-307-7183. SUPPLEMENTARY INFORMATION: Section 1903 of the Anabolic Steroids Control Act of 1990 (ASCA) (title XIX of Pub. L. 101-647) provides that the Attorney General may exempt products which contain anabolic steroids from all or any part of the Controlled Substances Act (CSA) (21 U.S.C. 801 et seq.) if the products have no significant potential for abuse. The procedure for implementing this section of the ASCA was published by the DEA on Friday, August 30, 1991, (56 FR 42935). The purpose of this rule is to identify two products which meet the exempt anabolic steroid product criteria. The Director, Office of Diversion Control, having reviewed the applications, the recommendations of the Secretary of the Department of Health and Human Services, and other relevant information, finds that each of the products described below has no significant potential for abuse because of its concentration, preparation, mixture or delivery system. Interested persons are invited to submit their comments in writing in regard to this interim rule. The listing of these products in 21 CFR 1308.34 relieves persons who handle them in the course of legitimate business from the registration, records, reports, prescription, physical security, import, and export requirements associated with Schedule III substances. Accordingly, the Director certifies that this action will have no impact on the ability of small businesses to compete and he therefore determines that no regulatory flexibility analysis is required. This action has been analyzed in accordance with the principles and criteria contained in E.O. 12612, and it has been determined that this matter does not have sufficient federalism implications to require the preparation of a Federalism Assessment. It has been determined that drug control matters are not subject to review by the Office of Management and Budget (OMB) pursuant to the provisions of E.O. 12291. Accordingly, this action is not subject to those provisions of E.O. 12778 which are contingent upon review by OMB. Nevertheless, the Director has determined that this is not a "major rule,'' as that term is used in E.O. 12291, and that it would otherwise meet the applicable standards of sections 2(a) and 2(b)(2) of E.O. 12778. List of Subjects in 21 CFR Part 1308 Administrative practice and procedure, Drug traffic control, Narcotics, Prescription drugs. Under the authority vested in the Attorney General by title XIX of Public Law 101-647, as delegated to the Administrator of the DEA pursuant to 21 U.S.C. 871(a) and 28 CFR 0.100, the Director of the Office of Diversion Control hereby amends 21 CFR part 1308 as set forth below: PART 1308-[AMENDED] 1. The authority citation for 21 CFR part 1308 continues to read as follows: Authority: 21 U.S.C. 811, 812, 871(b) unless otherwise noted. 2. Section 1308.34 is amended by adding two new entries to the Table of Exempt Anabolic Steroid Products, to be placed in alphabetical order first by Trade Name and then by Company, to read as follows: sec 1308.34 Exempt anabolic steroid products. * * * * * Table of Exempt Anabolic Ster oid Products ------------------------------------------------------------------------------- -------------------------------------------------------------- Trade name Company NDC No. Form Ingredients Quantity ------------------------------------------------------------------------------- -------------------------------------------------------------- * * * * * * * Testosterone Cypionate- Estradiol Cypionate Injection Testosterone Cypionate- The Upjohn Co., Kalamazoo, 0009-0253 Vial .
.......... Testosterone Cypionate ... 50 mg/ml. Estradiol Cypionate Injection. MI Estradiol Cypionate ...... 2 mg/ml. * * * * * * * Tilapia Sex Reversal Feed Zeigler Brothers, Inc., Plast ic Bags ... Methyltestosterone Fish 60 mg/1 kg. (Investigational). Gardners, PA feed * * * * * * * ------------------------------------------------------------------------------- -------------------------------------------------------------- Dated: June 22, 1993. Gene R. Haislip, Director, Office of Diversion Control, Drug Enforcement Administration. [FR Doc. 93-15181 Filed 6-28-93; 8:45 am] BILLING CODE 4410-09-M .