Propecia 78206-0152
Generic: Finasteride
Product NDC
78206-0152- Manufacturer
- Organon Llc
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- June 1, 2021
- Listing Expires
- December 31, 2026
- Application
- NDA020788
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Finasteride | 1 mg/1 |
Drug Class
5-alpha Reductase Inhibitor [EPC]5-alpha Reductase Inhibitor [EPC]5-alpha Reductase Inhibitors [MoA]
Packaging Options(2)
30 TABLET, FILM COATED in 1 BOTTLE (78206-152-01)
90 TABLET, FILM COATED in 1 BOTTLE (78206-152-02)