Federal brief
Bulk Manufacturer of Controlled Substances Application: Irvine Labs, Inc.
Publisher-desk brief on Drug Enforcement Administration FR 2026-19803 (2026-09-28). Use the filing for dates and comment paths.
DEA posted a bulk-manufacturer registration application that controlled-substance supply desks will treat as a calendar item, not a curiosity.
These manufacturer filings do not rewrite street policy overnight — they do change who may lawfully produce which schedules at which sites.
Filing abstract (agency text): Irvine Labs, Inc. 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.
Pharmacy supply counsel and manufacturing compliance leads: confirm the applicant name, schedules, and comment window in the FR PDF before you brief procurement.
Federal Register filing: https://www.federalregister.gov/documents/2026/09/28/2026-19803/bulk-manufacturer-of-controlled-substances-application-irvine-labs-inc
This is a Notice Nearby publisher-desk Federal brief — a short in-house summary of a public federal filing. It is not official agency minutes, not a newspaper story, and not Legal Publication. It does not satisfy a statutory notice requirement.
Source: the official public federal record 2026-19803 · Federal Register · 2026-19803 · 2026-19803.
This is a Notice Nearby publisher-desk Federal brief — a short in-house summary of a public federal filing. It is not official agency minutes, not a newspaper story, and not Legal Publication. It does not satisfy a statutory notice requirement.