# Nitazoxanide

NDC: 13517-135
Generic name: Nitazoxanide
Labeler / Manufacturer: e5 Pharma, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20260126

FDA application: ANDA214844

## 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:"13517-135"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=13517-135
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=40a7cc30-76cd-49fe-965a-7823c4140d0f