FDA NDC Directory · JSON-LD · Markdown

METRONIDAZOLE

NDC 61919-032 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerDirect_Rx
Marketing categoryAbbreviated NDA (generic) · App ANDA203458
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsMETRONIDAZOLE (500 mg/1)
Marketing started20190821
Package count1

External sources

Source: openFDA. Public-domain (CC0).