FDA NDC Directory · JSON-LD · Markdown

Nitazoxanide

NDC 13517-135 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / Manufacturere5 Pharma, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA214844
Dosage form / routeTABLET · ORAL
Active ingredientsNITAZOXANIDE (500 mg/1)
Marketing started20260126
Package count1

External sources

Source: openFDA. Public-domain (CC0).