Finasteride 47335-0714
Product NDC
47335-0714- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- November 23, 2022
- Listing Expires
- December 31, 2026
- Application
- ANDA090508
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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(5)
100 TABLET, FILM COATED in 1 BOTTLE (47335-714-08)
1000 TABLET, FILM COATED in 1 BOTTLE (47335-714-18)
90 TABLET, FILM COATED in 1 BOTTLE (47335-714-81)
30 TABLET, FILM COATED in 1 BOTTLE (47335-714-83)
100 TABLET, FILM COATED in 1 BOTTLE (47335-714-88)