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Metronidazole

NDC 65862-694 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAurobindo Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA203974
Dosage form / routeTABLET · ORAL
Active ingredientsMETRONIDAZOLE (250 mg/1)
Marketing started20150529
Package count5

External sources

Source: openFDA. Public-domain (CC0).