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Metronidazole

NDC 46708-021 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Labeler / ManufacturerAlembic Pharmaceuticals Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA090222
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsMETRONIDAZOLE (750 mg/1)
Marketing started20100507
Package count4

External sources

Source: openFDA. Public-domain (CC0).