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Minocycline Hydrochloride

NDC 67877-577 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Labeler / ManufacturerAscend Laboratories, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA204453
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsMINOCYCLINE HYDROCHLORIDE (135 mg/1)
Marketing started20160930
Package count4

External sources

Source: openFDA. Public-domain (CC0).