Finasteride 00904-6830
Product NDC
00904-6830- Manufacturer
- Major Pharmaceuticals
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- June 13, 2015
- Listing Expires
- December 31, 2026
- Application
- ANDA090061
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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(2)
50 BLISTER PACK in 1 CARTON (0904-6830-06) / 1 TABLET, FILM COATED in 1 BLISTER PACK
100 BLISTER PACK in 1 CARTON (0904-6830-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK