NDC 71335-1530 – Finasteride
Finasteride 5 mg/1 · Tablet, Film Coated · Oral
Product NDC71335-1530
Product details
- Brand name
- Finasteride
- Generic name
- Finasteride
- Labeler
- Bryant Ranch Prepack
- 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 (6)
| Package NDC | Description | Since |
|---|---|---|
| 71335-1530-1 | 100 TABLET, FILM COATED in 1 BOTTLE (71335-1530-1) | Dec 28, 2021 |
| 71335-1530-2 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-1530-2) | Mar 6, 2020 |
| 71335-1530-3 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-1530-3) | Dec 28, 2021 |
| 71335-1530-4 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-1530-4) | Mar 20, 2020 |
| 71335-1530-5 | 500 TABLET, FILM COATED in 1 BOTTLE (71335-1530-5) | Dec 28, 2021 |
| 71335-1530-6 | 180 TABLET, FILM COATED in 1 BOTTLE (71335-1530-6) | Dec 28, 2021 |
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