FDA NDC Directory · JSON-LD · Markdown

Metronidazole

NDC 72789-007 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerPD-Rx Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA079067
Dosage form / routeTABLET · ORAL
Active ingredientsMETRONIDAZOLE (500 mg/1)
Marketing started20161201
Package count8

External sources

Source: openFDA. Public-domain (CC0).