NDC 57237-062 – Finasteride
Finasteride 5 mg/1 · Tablet, Film Coated · Oral
Product NDC57237-062
Product details
- Brand name
- Finasteride
- Generic name
- Finasteride
- Labeler
- Rising Pharma Holdings, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA078341
- Marketed since
- October 30, 2007
- Listing expires
- December 31, 2027
- Pharmacologic class
- 5-alpha Reductase Inhibitor
Active ingredients
- Finasteride 5 mg/1
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 57237-062-05 | 500 TABLET, FILM COATED in 1 BOTTLE (57237-062-05) | Oct 30, 2007 |
| 57237-062-30 | 30 TABLET, FILM COATED in 1 BOTTLE (57237-062-30) | Oct 30, 2007 |
| 57237-062-90 | 90 TABLET, FILM COATED in 1 BOTTLE (57237-062-90) | Oct 30, 2007 |
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