NDC 71205-767 – Finasteride
Finasteride 5 mg/1 · Tablet, Film Coated · Oral
Product NDC71205-767
Product details
- Brand name
- Finasteride
- Generic name
- Finasteride
- Labeler
- Proficient Rx LP
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA204304
- Marketed since
- January 5, 2017
- 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 |
|---|---|---|
| 71205-767-30 | 30 TABLET, FILM COATED in 1 BOTTLE (71205-767-30) | Feb 23, 2023 |
| 71205-767-60 | 60 TABLET, FILM COATED in 1 BOTTLE (71205-767-60) | Feb 23, 2023 |
| 71205-767-90 | 90 TABLET, FILM COATED in 1 BOTTLE (71205-767-90) | Feb 23, 2023 |
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