The Federal Register

Manufacturer of Controlled Substances; Notice of Registration

Tue, Nov 29 2005 11:00:00 GMT

By Notice dated June 2, 2005, and published in the Federal Register on June 10, 2005, (70 FR 33923), Research Triangle Institute, Kenneth H. Davis Jr., Herman Building, P.O. Box 12194, East Institute Drive, Research Triangle Park, North Carolina 27709, made application by renewal to the Drug Enforcement Administration (DEA) to be registered as a bulk manufacturer of the basic classes of controlled substances listed in Schedules I and II:
Drug Schedule Marihuana (7360)........................... I

Cocaine (9041)............................. II

The Institute will manufacture small quantities of cocaine and marihuana derivatives for use by their customers primarily in analytical kits, reagents and reference standards.

No comments or objections have been received. DEA has considered the factors in 21 U.S.C. 823(a) and determined that the registration of Research Triangle Institute to manufacture the listed basic classes of controlled subs

Importer of Controlled Substances; Notice of Registration

Tue, Nov 29 2005 11:00:00 GMT

By Notice dated March 29, 2005 and published in the Federal Register on April 6, 2005, (70 FR 1747217473), Penick Corporation, 158 Mount Olivet Avenue, Newark, New Jersey 07114, made application by renewal to the Drug Enforcement Administration (DEA) to be registered as an importer of the basic class of controlled substances listed in Schedule II.
Drug Schedule Coca Leaves (9040)......................... II
Raw Opium (9600)........................... II
Poppy Straw (9650)......................... II

Concentrate of Poppy Straw (9670).......... II

The company plans to import the listed controlled substances to manufacturer bulk controlled substances and noncontrolled substance flavor extracts.

Following the Notice of Application publication on April 6, 2005, (70 FR 1747217473), Penick Corporation, 158 Mount Olivet Avenue, Newark, New Jersey 07114, relocated its operations to 33 Industrial Park Road, Pennsville, New Jersey 08070 on May

Manufacturer of Controlled Substances; Notice of Registration

Tue, Nov 29 2005 11:00:00 GMT

By Notice dated April 14, 2005, and published in the Federal Register on April 25, 2005 (70 FR 10683), Penick Corporation, Inc., 158 Mount Olivet Avenue, Newark, New Jersey, 07114, made application by renewal to the Drug Enforcement Administration (DEA) to be registered as a bulk manufacturer of the basic class of controlled substances listed in Schedule II:
Drug Schedule Cocaine (9041)............................. II
Codeine (9050)............................. II
Dihydrocodeine (9120)...................... II
Oxycodone (9143)........................... II
Hydromorphone (9150)....................... II
Ecgonine (9180)............................ II
Hydrocodone (9193)......................... II
Morphine (9300)............................ II
Thebaine (9333)............................ II

Oxymorphone (9652)......................... II

The company plans to manufacture the listed bulk controlled substances in bulk for distribution to its c

Manufacturer of Controlled Substances; Notice of Application

Tue, Nov 29 2005 11:00:00 GMT

Pursuant to Section 1301.33(a) of Title 21 of the Code of Federal Regulations (CFR), this is notice that on March 3, 2005, American Radiolabeled Chemicals, Inc., 101 Arc Drive, St. Louis, Missouri 63146, made application by renewal to the Drug Enforcement Administration (DEA) for registration as a bulk manufacturer of the basic classes of controlled substances listed in Schedules I and II:
Drug Schedule Gamma hydroxybutyric acid (2010). I
Dimethyltryptamine (7435).................. I
Dihydromorphine (9145)..................... I
Amphetamine (1100)......................... II
Methamphetamine (1105)..................... II
Lysergic acid diethylamide (7315). II
Phencyclidine (7471)....................... II
Phenylacetone (8501)....................... II
Cocaine (9041)............................. II
Codeine (9050)............................. II
Oxycodone (9143)........................... II
Hydromorphone (9150).

Manufacturer of Controlled Substances; Notice of Application

Tue, Nov 29 2005 11:00:00 GMT

Pursuant to section 1301.33(a) of Title 21 of the Code of Federal Regulations (CFR), this is notice that on May 6, 2005, Chemic Laboratories, Inc., 480 Neponset Street, Building 7C, Canton, Massachusetts 02021, made application by renewal to the Drug Enforcement Administration (DEA) to be registered as a bulk manufacturer of Cocaine (9041), a basic class of controlled substance listed in Schedule II.

The company plans to manufacture small quantities of a cocaine derivative for distribution to its customers for the purpose of research.

Any other such applicant and any person who is presently registered with DEA to manufacture such a substance
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may file comments or objections to the issuance of the proposed registration pursuant to 21 CFR 1301.33(a).

Any such written comments or objections being sent via regular mail may be addressed, in quintuplicate, to the Deputy Assistant Administrator, Office of Diversion Control, Drug Enforcement Administration, Washington, DC 2

Manufacturer of Controlled Substances; Notice of Application

Tue, Nov 29 2005 11:00:00 GMT

Pursuant to Section 1301.33(a) of Title 21 of the Code of Federal Regulations (CFR), this is notice that on April 18, 2005, Dade Behring Inc., 100 GBE Drive, MS514, Post Office Box 6101, Attention: RA/QS, Newark, Delaware 197146101, made application by renewal to the Drug Enforcement Administration (DEA) to be registered as a bulk manufacturer of the basic classes of controlled substances listed in Schedules I and II:
Drug Schedule Tetrahydrocannabionols (7370).............. I
Benzoylecgonine (9180)..................... II

Morphine (9300)............................ II

The company plans to produce the listed controlled substances in bulk to be used in the manufacture of reagents and drug calibrator/ controls for DEA exempt products.

Any other such applicant and any person who is presently registered with DEA to manufacture such a substance may file comments or objections to the issuance of the proposed registration pursuant to 21 CFR

Manufacturer of Controlled Substances; Notice of Application

Tue, Nov 29 2005 11:00:00 GMT

Pursuant to Section 1301.33(a) of Title 21 of the Code of Federal Regulations (CFR), this is notice that on May 13, 2005, Dade Behring, Inc., Regulatory Affairs, Quality Systems, 20400 Mariani Avenue, Cupertino, California 95014, made application by renewal to the Drug Enforcement Administration (DEA) for registration as a bulk manufacturer of the basic classes of controlled substances listed in Schedule I and II:
Drug Schedule Tetrahydrocannabionols (7370).............. I
Benzoylecgonine (9180)..................... II

Morphine (9300)............................ II

The company plans to produce the listed controlled substances in bulk to be used in the manufacture of reagents and drug calibrator/ controls for DEA exempt products.

Manufacturer of Controlled Substances; Notice of Application

Tue, Nov 29 2005 11:00:00 GMT

Pursuant to Section 1301.33(a) of Title 21 of the Code of Federal Regulations (CFR), this is notice that on August 10, 2005, ISP, Freetown Fine Chemicals, Inc., 238 South Main Street, Assonet, Massachusetts 02702, made application by renewal to the Drug Enforcement Administration (DEA) for registration as a bulk manufacturer of the basic classes of controlled substances listed in Schedules I and II:
Drug Schedule 2,5Dimethoxyamphetamine (7396)............ I
Amphetamine (1100)......................... II

Phenylacetone (8501)....................... II

The company plans to manufacture phenylacetone to be used in the manufacture of amphetamine for distribution to its customers. The bulk 2,5dimethoxyamphetamine will be used for conversion into non controlled substances.

Any other such applicant and any person who is presently registered with DEA to manufacture such a substance may file comments or objections to the issuance of the proposed