FDA NDC Directory · JSON-LD · Markdown

Minocycline Hydrochloride

NDC 0591-5694 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerActavis Pharma, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA063181
Dosage form / routeCAPSULE · ORAL
Active ingredientsMINOCYCLINE HYDROCHLORIDE (50 mg/1)
Marketing started19920201
Package count2

External sources

Source: openFDA. Public-domain (CC0).