NDC 0093-7355 – Finasteride
Finasteride 5 mg/1 · Tablet, Film Coated · Oral
Product NDC0093-7355
Product details
- Brand name
- Finasteride
- Generic name
- Finasteride
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA076511
- Marketed since
- December 15, 2006
- Marketing end
- September 30, 2026
- Pharmacologic class
- 5-alpha Reductase Inhibitor
Active ingredients
- Finasteride 5 mg/1
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 0093-7355-05 | 500 TABLET, FILM COATED in 1 BOTTLE (0093-7355-05) | Mar 14, 2008 |
| 0093-7355-56 | 30 TABLET, FILM COATED in 1 BOTTLE (0093-7355-56) | Dec 15, 2006 |
| 0093-7355-98 | 90 TABLET, FILM COATED in 1 BOTTLE (0093-7355-98) | Feb 22, 2007 |
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