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Minocycline Hydrochloride

NDC 68180-381 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerLupin Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA091424
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsMINOCYCLINE HYDROCHLORIDE (135 mg/1)
Marketing started20120214
Package count0

External sources

Source: openFDA. Public-domain (CC0).