Federal Register #DEA-1735

DEA Notice: Veranova, L.P. Application for Bulk Manufacturing of Controlled Substances

This opportunity concerns the Drug Enforcement Administration (DEA) issuing a notice about Veranova, L.P.'s application to become a bulk manufacturer of controlled substances. - Government Buyer: - U.S. Department of Justice, Drug Enforcement Administration (DEA) - OEM/Vendor: - Veranova, L.P. (applicant for manufacturing registration) - Products/Services Requested: - Bulk manufacturing of basic classes of controlled substances, including: - Lysergic Acid Diethylamide (LSD) - 3,4-Methylenedioxymethamphetamine (MDMA) - Dimethyltryptamine (DMT) - Amphetamine - Methylphenidate - Nabilone - Hydrocodone - Levorphanol - Thebaine - Alfentanil - Remifentanil - Sufentanil - No specific part numbers or quantities provided - Unique/Notable Requirements: - Registration is for bulk manufacturing and analytical testing at another DEA-registered facility - Public comments and objections are invited regarding the proposed registration - OEM Highlight: - Veranova, L.P. is the applicant seeking DEA registration as a bulk manufacturer

Description

Veranova, L.P. has applied to be registered as a bulk manufacturer of basic classes of controlled substances. The application involves the registration to support manufacturing and analytical testing activities at another DEA-registered manufacturing facility. Comments and objections to the proposed registration can be submitted electronically on or before August 31, 2026. A written request for a hearing can also be filed by the same date.

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