FDA NDC Directory · JSON-LD · Markdown

Metronidazole

NDC 68001-364 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerBluePoint Laboratories
Marketing categoryAbbreviated NDA (generic) · App ANDA203458
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsMETRONIDAZOLE (250 mg/1)
Marketing started20180801
Package count1

External sources

Source: openFDA. Public-domain (CC0).