Bulk Manufacturer of Controlled Substances Application: Veranova, L.P.

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Choosing an item from suggestions will bring you directly to the content. Thank you for taking the time to create a comment. Your input is important. Once you have filled in the required fields below you can preview and/or submit your comment to the Justice Department for review. All comments are considered public and will be posted online once the Justice Department has reviewed them. Registered bulk manufacturers of the affected basic class(es), and applicants, therefore, may submit electronic comments on, or objections to the issuance of the proposed registration on or before August 14, 2026. Such persons may also file a written request for a hearing on the application on or before August 14, 2026. Table of Contents Enhanced Content - Table of Contents This table 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. 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Use the PDF linked in the document sidebar for the official electronic format. AGENCY: Drug Enforcement Administration, Justice. ( printed page 36011) ACTION: Notice of application. SUMMARY: Veranova, L.P., has applied to be registered as a bulk manufacturer of basic class(es) of controlled substance(s). Refer to Supplementary Information listed below for further drug information. DATES: Registered bulk manufacturers of the affected basic class(es), and applicants, therefore, may submit electronic comments on, or objections to the issuance of the proposed registration on or before August 14, 2026. Such persons may also file a written request for a hearing on the application on or before August 14, 2026. ADDRESSES: The Drug Enforcement Administration requires that all comments be submitted electronically through the Federal eRulemaking Portal, which provides the ability to type short comments directly into the comment field on the web page or attach a file for lengthier comments. Please go to https://www.regulations.gov and follow the online instructions at that site for submitting comments. Upon submission of your comment, you will receive a Comment Tracking Number. Please be aware that submitted comments are not instantaneously available for public view on https://www.regulations.gov. If you have received a Comment Tracking Number, your comment has been successfully submitted and there is no need to resubmit the same comment. SUPPLEMENTARY INFORMATION: In accordance with 21 CFR 1301.33(a), this is notice that on May 14, 2026, Veranova, L.P., 2003 Nolte Drive, West Deptford New Jersey 08066-1727, applied to be registered as a bulk manufacturer of the following basic class(es) of controlled substance(s): Controlled Substance Gamma Hydroxybutyric Acid Marihuana Tetrahydrocannabinols 3,4-Methylenedioxymethamphetamine Psilocybin Dihydromorphine Difenoxin Fentanyl-Related Substance Amphetamine Methamphetamine Lisdexamfetamine Methylphenidate Nabilone 4-Anilino-N-phenethyl-4-piperidine (ANPP) Norfentanyl Cocaine Codeine Dihydrocodeine Oxycodone Hydromorphone Diphenoxylate Ecgonine Hydrocodone Levorphanol Meperidine Methadone Methadone intermediate Morphine Thebaine Opium tincture Oxymorphone Noroxymorphone Alfentanil Remifentanil Sufentanil Tapentadol Fentanyl The company plans to bulk manufacture the listed controlled substances for use as internal intermediates and for sale to its customers. No other activities for these drug codes are authorized for this registration.