# Finasteride

NDC: 71713-099
Generic name: Finasteride
Labeler / Manufacturer: Thirty Madison Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20210322

FDA application: ANDA207750

## Active ingredients

- FINASTERIDE: 1 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71713-099"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71713-099
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3fe7bdaa-b027-4da9-94ee-550bf28c63e1