Finasteride 55111-0171
Product NDC
55111-0171- Manufacturer
- Dr. Reddy's Laboratories Limited
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- January 2, 2013
- Listing Expires
- December 31, 2026
- Application
- ANDA076436
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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(4)
500 TABLET, FILM COATED in 1 BOTTLE (55111-171-05)
180 TABLET, FILM COATED in 1 BOTTLE (55111-171-18)
30 TABLET, FILM COATED in 1 BOTTLE (55111-171-30)
90 TABLET, FILM COATED in 1 BOTTLE (55111-171-90)