NDC 68071-3785 – Finasteride
Finasteride 5 mg/1 · Tablet, Film Coated · Oral
Product NDC68071-3785
Product details
- Brand name
- Finasteride
- Generic name
- Finasteride
- Labeler
- NuCare Pharmaceuticals, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA078341
- Marketed since
- October 30, 2007
- Listing expires
- December 31, 2026
- Pharmacologic class
- 5-alpha Reductase Inhibitor
Active ingredients
- Finasteride 5 mg/1
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 68071-3785-2 | 120 TABLET, FILM COATED in 1 BOTTLE (68071-3785-2) | Jan 23, 2025 |
| 68071-3785-6 | 60 TABLET, FILM COATED in 1 BOTTLE (68071-3785-6) | Oct 9, 2025 |
| 68071-3785-8 | 180 TABLET, FILM COATED in 1 BOTTLE (68071-3785-8) | Jan 23, 2025 |
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