# Benznidazole

NDC: 0642-7464
Generic name: benznidazole
Labeler / Manufacturer: Exeltis USA, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20180330

FDA application: NDA209570

## Active ingredients

- BENZNIDAZOLE: 100 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0642-7464"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0642-7464
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8983d6a0-f63f-4f8e-bba4-38223f39e29b