Federal Register #DEA1735

DEA Registration for Bulk Manufacturing of Controlled Substances by Veranova, L.P.

The Drug Enforcement Administration (DEA), part of the Department of Justice, is overseeing a registration process for bulk manufacturing of controlled substances: - Government Buyer: - Drug Enforcement Administration (DEA), Department of Justice - OEM/Vendor: - Veranova, L.P. - Products/Services Requested: - Registration for bulk manufacturing of the following controlled substances (no part numbers or quantities specified): - Lysergic Acid Diethylamide (LSD) - 3,4-Methylenedioxymethamphetamine (MDMA) - Dimethyltryptamine (DMT) - Amphetamine - Methylphenidate - Nabilone - Hydrocodone - Levorphanol - Thebaine - Alfentanil - Remifentanil - Sufentanil - Unique/Notable Requirements: - Registration is strictly for manufacturing and analytical testing at DEA-registered facilities - No other activities are authorized for these drug codes - Compliance with DEA regulations is mandatory - No specific contract value, period of performance, or part numbers are provided, as this is a registration for manufacturing capability, not a purchase.

Description

Veranova, L.P. has applied to be registered as a bulk manufacturer of basic classes of controlled substances. The company plans to bulk manufacture the listed controlled substances to support manufacturing and analytical testing activities at its other DEA-registered manufacturing facility. No other activities for these drug codes are authorized for this registration. Registered bulk manufacturers and applicants may submit electronic comments or objections to the issuance of the proposed registration by August 31, 2026, and may also file a written request for a hearing by the same date.

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