Finasteride 65862-0149
Product NDC
65862-0149- Manufacturer
- Aurobindo Pharma Limited
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- October 30, 2007
- Listing Expires
- December 31, 2027
- Application
- ANDA078341
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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(4)
100 TABLET, FILM COATED in 1 BOTTLE (65862-149-01)
500 TABLET, FILM COATED in 1 BOTTLE (65862-149-05)
30 TABLET, FILM COATED in 1 BOTTLE (65862-149-30)
90 TABLET, FILM COATED in 1 BOTTLE (65862-149-90)