# Finasteride

NDC: 71335-0433
Generic name: finasteride
Labeler / Manufacturer: Bryant Ranch Prepack
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20100528

FDA application: ANDA090121

## Active ingredients

- FINASTERIDE: 5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71335-0433"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71335-0433
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ef9c0b23-4736-4fb0-862c-c2a4d644e0d6