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Minocycline Hydrochloride

NDC 65862-885 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Labeler / ManufacturerAurobindo Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA202261
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsMINOCYCLINE HYDROCHLORIDE (105 mg/1)
Marketing started20160613
Package count4

External sources

Source: openFDA. Public-domain (CC0).