# PROPECIA

NDC: 78206-152
Generic name: finasteride
Labeler / Manufacturer: Organon LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20210601

FDA application: NDA020788

## 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:"78206-152"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=78206-152
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6f904709-65aa-44ce-b144-b4c8a0416e36