FDA NDC Directory · JSON-LD · Markdown

Nitazoxanide

NDC 70954-934 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerANI Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA214844
Dosage form / routeTABLET · ORAL
Active ingredientsNITAZOXANIDE (500 mg/1)
Marketing started20250305
Package count1

External sources

Source: openFDA. Public-domain (CC0).