Manufacturer of Controlled Substances; Notice of Registration

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Federal RegisterDec 5, 2000
65 Fed. Reg. 75956 (Dec. 5, 2000)

By notice dated August 21, 2000, and published in the Federal Register on September 6, 2000, (65 FR 54067), Applied Science Labs, Division of Alltech Associates, Inc., 2701 Carolean Industrial Drive, P.O. Box 440, State College, Pennsylvania 16801, 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 below:

Drug Schedule
Methcathinone (1237) I
N-Ethylamphetamine (1475) I
N,N-Dimethylamphetamine (1480) I
4-Methylaminorex (cis isomer) (1590) I
Lysergic acid dyethylamide (7315) I
Mescaline (7381) I
3,4-Methylenedioxyamphetamine (7400) I
N-Hydroxy-3,4-methylenedioxyamphetamine (7402) I
3,4-Methylenedioxy-N-ethylamphetamine (7404) I
3,4-Methylenedioxymethamphetamine (7405) I
N-Ethyl-1-phenylcyclohexylamine (7455) I
1-(1-Phenylcyclohexyl)pyrrolidine (7458) I
1-[1-(2-Thienyl)cyclohexyl]piperidine (7470) I
Dihydromorphine (9145) I
Normorphine (9313) I
1-Phenylcyclohexylamine (7460) II
Phencyclidine (7471) II
Phenylacetone (8501) II
1-Piperidinocyclohexanecarbonitrile (8603) II
Cocaine (9041) II
Codeine (9050) II
Dihydrocodeine (9120) II
Benzoylecgonine (9180) II
Morphine (9300) II
Noroxymorphone (9668) II

The firm plans to manufacture small quantities of the listed controlled substances for reference standards.

No comments or objections were received. DEA has considered the factors in title 21, United States Code, section 823(a) and determined that the registration of Applied Science Labs to manufacture the listed controlled substances is consistent with the public interest at this time. DEA has investigated Applied Science Labs on a regular basis to ensure that the company's continued registration is consistent with the public interest. These investigations have included inspection and testing of the company's physical security systems, audits of the company's records, verification of the company's compliance with state and local laws, and a review of the company's background and history. Therefore, pursuant to 21 U.S.C. 823 and 28 CFR 0.100 and 0.104, the Deputy Assistant Administrator, Office of Diversion Control, hereby orders that the application submitted by the above firm for registration as a bulk manufacturer of the basic classes of controlled substances listed above is granted.

Dated: November 20, 2000.

John H. King,

Deputy Assistant Administrator, Office of Diversion Control, Drug Enforcement Administration.

[FR Doc. 00-30935 Filed 12-4-00; 8:45 am]

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