Legal Status
Legal Status
Notice
Manufacturer of Controlled Substances; Notice of Application
A Notice by the Drug Enforcement Administration on
Document Details
Information about this document as published in the Federal Register.
- Printed version:
- Publication Date:
- 04/15/2003
- Agencies:
- Drug Enforcement Administration
- Document Type:
- Notice
- Document Citation:
- 68 FR 18262
- Page:
- 18262 (1 page)
- Document Number:
- 03-9227
Document Details
-
Enhanced Content - Table of Contents
This tables of contents is a navigational tool, processed from the headings within the legal text of Federal Register documents. This repetition of headings to form internal navigation links has no substantive legal effect.
There is no table of contents available for this document.Enhanced Content - Table of Contents
-
Enhanced Content - Submit Public Comment
- This feature is not available for this document.
Enhanced Content - Submit Public Comment
-
Enhanced Content - Read Public Comments
- This feature is not available for this document.
Enhanced Content - Read Public Comments
-
Enhanced Content - Sharing
- Shorter Document URL
- https://www.federalregister.gov/d/03-9227 https://www.federalregister.gov/d/03-9227
Enhanced Content - Sharing
-
Enhanced Content - Document Tools
These tools are designed to help you understand the official document better and aid in comparing the online edition to the print edition.
-
These markup elements allow the user to see how the document follows the Document Drafting Handbook that agencies use to create their documents. These can be useful for better understanding how a document is structured but are not part of the published document itself.
Display Non-Printed Markup Elements
Enhanced Content - Document Tools
-
-
Enhanced Content - Developer Tools
This document is available in the following developer friendly formats:
- JSON: Normalized attributes and metadata
- XML: Original full text XML
- MODS: Government Publishing Office metadata
More information and documentation can be found in our developer tools pages.
Enhanced Content - Developer Tools
Published Document
This document has been published in the Federal Register. Use the PDF linked in the document sidebar for the official electronic format.
Pursuant to Section 1301.33(a) of Title 21 of the Code of Federal Regulations (CFR), this is notice that on April 25, 2002, Cody Laboratories, Inc., 331 33rd Street, Cody, Wyoming 82414, made application by renewal, and on March 5, 2003, by letter to the Drug Enforcement Administration (DEA) for registration as a bulk manufacturer of the basic classes of Schedule II of controlled substances listed below:
| Drug | Schedule |
|---|---|
| Dihydromorphine (9145) | II |
| Methamphetamine (1105) | II |
| Amphetamine (1100) | II |
| Amobarbital (2125) | II |
| Pentobarbital (2270) | II |
| Secobarbital (2315) | II |
| Phenylacetone (8501) | II |
| Oxycodone (9143) | II |
| Hydromorphone (9150) | II |
| Fentanyl (9801) | II |
The firm plans to produce bulk products for distribution to its customers.
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: Drug Operations Section, Domestic Drug Unit (ODOD) and must be filed no later than June 16, 2003.
Start SignatureDated: April 3, 2003.
Laura M. Nagel,
Deputy Assistant Administrator, Office of Diversion Control, Drug Enforcement Administration.
[FR Doc. 03-9227 Filed 4-14-03; 8:45 am]
BILLING CODE 4410-09-M