# Finasteride

NDC: 63187-265
Generic name: finasteride
Labeler / Manufacturer: Proficient Rx LP
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

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63187-265"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63187-265
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e9ea2f77-11c3-4dbf-bdc4-d1b0e7437990