# Pretomanid

NDC: 49502-476
Generic name: Pretomanid
Labeler / Manufacturer: Viatris Specialty LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20191107

FDA application: NDA212862

## Active ingredients

- PRETOMANID: 200 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"49502-476"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=49502-476
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f1906fc9-cb3c-4e13-8a4a-da76100c1bf3