# Nitazoxanide

NDC: 70954-934
Generic name: Nitazoxanide
Labeler / Manufacturer: ANI Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20250305

FDA application: ANDA214844

## Active ingredients

- NITAZOXANIDE: 500 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70954-934"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70954-934
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=cd3652fa-a183-4fb6-9a21-73fbeba6fc4b