Finasteride 71335-0433
Product NDC
71335-0433- Manufacturer
- Bryant Ranch Prepack
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- May 28, 2010
- Listing Expires
- December 31, 2026
- Application
- ANDA090121
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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(6)
100 TABLET, FILM COATED in 1 BOTTLE (71335-0433-1)
30 TABLET, FILM COATED in 1 BOTTLE (71335-0433-2)
60 TABLET, FILM COATED in 1 BOTTLE (71335-0433-3)
90 TABLET, FILM COATED in 1 BOTTLE (71335-0433-4)
500 TABLET, FILM COATED in 1 BOTTLE (71335-0433-5)
180 TABLET, FILM COATED in 1 BOTTLE (71335-0433-6)