Finasteride 68071-2999
Product NDC
68071-2999- Manufacturer
- Nucare Pharmaceuticals,inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- January 5, 2017
- Listing Expires
- December 31, 2026
- Application
- ANDA204304
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Finasteride | 5 mg/1 |
Drug Class
5-alpha Reductase Inhibitor [EPC]5-alpha Reductase Inhibitor [EPC]5-alpha Reductase Inhibitors [MoA]
Packaging Options(1)
90 TABLET, FILM COATED in 1 BOTTLE (68071-2999-9)