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Metronidazole

NDC 15955-389 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAlembic Labs LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA208681
Dosage form / routeTABLET · ORAL
Active ingredientsMETRONIDAZOLE (500 mg/1)
Marketing started20190626
Package count2

External sources

Source: openFDA. Public-domain (CC0).