# Finasteride

NDC: 35573-400
Generic name: Finasteride
Labeler / Manufacturer: Burel Pharmaceuticals, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20180713

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:"35573-400"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=35573-400
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c8516eaa-98d0-4eb1-bc65-aa765baea5db