# Nitazoxanide

NDC: 64980-526
Generic name: Nitazoxanide
Labeler / Manufacturer: Rising Pharma Holdings, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20201127

FDA application: ANDA213820

## Active ingredients

- NITAZOXANIDE: 500 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"64980-526"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=64980-526
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c0dc0656-3c46-43f9-adea-5285c522cef8