NDC 55111-172 – Finasteride
Finasteride 5 mg/1 · Tablet · Oral
Product NDC55111-172
Product details
- Brand name
- Finasteride
- Generic name
- Finasteride
- Labeler
- Dr. Reddy's Laboratories Limited
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA076437
- Marketed since
- February 28, 2007
- Listing expires
- December 31, 2026
- Pharmacologic class
- 5-alpha Reductase Inhibitor
Active ingredients
- Finasteride 5 mg/1
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 55111-172-01 | 100 TABLET in 1 BOTTLE (55111-172-01) | Feb 28, 2007 |
| 55111-172-05 | 500 TABLET in 1 BOTTLE (55111-172-05) | Feb 28, 2007 |
| 55111-172-30 | 30 TABLET in 1 BOTTLE (55111-172-30) | Feb 28, 2007 |
| 55111-172-78 | 10 BLISTER PACK in 1 CARTON (55111-172-78) / 10 TABLET in 1 BLISTER PACK (55111-172-79) | Feb 28, 2007 |
| 55111-172-90 | 90 TABLET in 1 BOTTLE (55111-172-90) | Feb 28, 2007 |
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