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Metronidazole

NDC 46708-429 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAlembic Pharmaceuticals Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA079067
Dosage form / routeTABLET · ORAL
Active ingredientsMETRONIDAZOLE (500 mg/1)
Marketing started20161201
Package count5

External sources

Source: openFDA. Public-domain (CC0).