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Metronidazole

NDC 70518-1536 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA203458
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsMETRONIDAZOLE (250 mg/1)
Marketing started20181015
Package count2

External sources

Source: openFDA. Public-domain (CC0).