# Finasteride

NDC: 17856-0090
Generic name: finasteride
Labeler / Manufacturer: Atlantic Biologicals Corps
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:"17856-0090"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=17856-0090
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=29e59387-120c-4367-9f87-75cb53b6460d