# AVODART

NDC: 80725-712
Generic name: dutasteride
Labeler / Manufacturer: Waylis Therapeutics LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: CAPSULE, LIQUID FILLED
Routes: ORAL
Marketing started: 20221215

FDA application: NDA021319

## Active ingredients

- DUTASTERIDE: .5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"80725-712"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=80725-712
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=960797b3-09b1-4d6a-8ece-8b5d918e93e4