NDC 68788-8749 – Finasteride
Finasteride 5 mg/1 · Tablet, Film Coated · Oral
Product NDC68788-8749
Product details
- Brand name
- Finasteride
- Generic name
- Finasteride
- Labeler
- Preferred Pharmaceuticals Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA078341
- Marketed since
- October 11, 2024
- 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 |
|---|---|---|
| 68788-8749-1 | 100 TABLET, FILM COATED in 1 BOTTLE (68788-8749-1) | Oct 11, 2024 |
| 68788-8749-3 | 30 TABLET, FILM COATED in 1 BOTTLE (68788-8749-3) | Oct 11, 2024 |
| 68788-8749-6 | 60 TABLET, FILM COATED in 1 BOTTLE (68788-8749-6) | Oct 11, 2024 |
| 68788-8749-9 | 90 TABLET, FILM COATED in 1 BOTTLE (68788-8749-9) | Oct 11, 2024 |
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