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minocycline hydrochloride

NDC 68382-552 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerZydus Pharmaceuticals (USA) Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA203553
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsMINOCYCLINE HYDROCHLORIDE (105 mg/1)
Marketing started20180307
Package count6

External sources

Source: openFDA. Public-domain (CC0).