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Start Preamble
Pursuant to § 1301.33(a) of Title 21 of the Code of Federal Regulations (CFR), this is notice that on October 24, 1999, High Standard Products, 1100 W. Florence Avenue, #B, Inglewood, California 90301, made application by renewal to the Drug Enforcement Administration (DEA) for registration as a bulk manufacturer of the basic classes of controlled substances listed below:
Drug Schedule Methaqualone (2565) I Lysergic acid diethylamide (7315) I Tetrahydrocannabinols (7370) I 3,4-Methylenedioxyamphetamine (7400) I 3,4-Methylenedioxy-N-ethylamphetamine (7404) I 3,4-Methylenedioxymethamphetamine (7405) I 4-Methoxyamphetamine (7411) I Heroin (9200) I 3-Methylfentanyl (9813) I Amphetamine (1100) II Methamphetamine (1105) II Secobarbital (2315) II Phencyclidine (7471) II Cocaine (9041) II Codeine (9050) II Hydromorphone (9150) II Diphenoxylate (9170) II Hydrocodone (9193) II Methadone (9250) II Morphine (9300) II Fentanyl (9801) II The firm plans to manufacture analytical reference standards.
Any other such applicant and any person who is presently registered with DEA to manufacture such substances may file comments or objections to the issuance of the proposed registration.
Any such comments or objections may be addressed, in quintuplicate, to the Deputy Assistant Administrator, Office of Diversion Control, Drug Enforcement Administration, United States Department of Justice, Washington, DC 20537, Attention: DEA Federal Register Representative (CCR), and must be filed no later than April 10, 2000.
Start SignatureDated: February 2, 2000.
John H. King,
Deputy Assistant Administrator, Office of Diversion Control, Drug Enforcement Administration.
[FR Doc. 00-3148 Filed 2-9-00; 8:45 am]
BILLING CODE 4410-09-M
Document Information
- Published:
- 02/10/2000
- Department:
- Drug Enforcement Administration
- Entry Type:
- Notice
- Document Number:
- 00-3148
- Pages:
- 6634-6634 (1 pages)
- PDF File:
- 00-3148.pdf