# Finasteride

NDC: 68788-6875
Generic name: Finasteride
Labeler / Manufacturer: Preferred Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20170123

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:"68788-6875"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68788-6875
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=74b90430-8ce1-470c-939c-685ca9dfd74f