NDC 65862-149 – Finasteride
Finasteride 5 mg/1 · Tablet, Film Coated · Oral
Product NDC65862-149
Product details
- Brand name
- Finasteride
- Generic name
- Finasteride
- Labeler
- Aurobindo Pharma Limited
- 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 (4)
| Package NDC | Description | Since |
|---|---|---|
| 65862-149-01 | 100 TABLET, FILM COATED in 1 BOTTLE (65862-149-01) | Oct 30, 2007 |
| 65862-149-05 | 500 TABLET, FILM COATED in 1 BOTTLE (65862-149-05) | Oct 30, 2007 |
| 65862-149-30 | 30 TABLET, FILM COATED in 1 BOTTLE (65862-149-30) | Oct 30, 2007 |
| 65862-149-90 | 90 TABLET, FILM COATED in 1 BOTTLE (65862-149-90) | Oct 30, 2007 |
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