# Finasteride

NDC: 76420-151
Generic name: Finasteride
Labeler / Manufacturer: Asclemed USA, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20131105

FDA application: ANDA203687

## 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:"76420-151"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=76420-151
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b2cac9e5-ea52-44b7-ae88-78e11a732904