NDC 71335-1898 – Finasteride
Finasteride 5 mg/1 · Tablet, Film Coated · Oral
Product NDC71335-1898
Product details
- Brand name
- Finasteride
- Generic name
- Finasteride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA204304
- Marketed since
- January 5, 2017
- Listing expires
- December 31, 2027
- Pharmacologic class
- 5-alpha Reductase Inhibitor
Active ingredients
- Finasteride 5 mg/1
Package NDC codes (6)
| Package NDC | Description | Since |
|---|---|---|
| 71335-1898-1 | 100 TABLET, FILM COATED in 1 BOTTLE (71335-1898-1) | Aug 20, 2026 |
| 71335-1898-2 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-1898-2) | Oct 15, 2021 |
| 71335-1898-3 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-1898-3) | Nov 9, 2021 |
| 71335-1898-4 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-1898-4) | Jun 21, 2021 |
| 71335-1898-5 | 500 TABLET, FILM COATED in 1 BOTTLE (71335-1898-5) | Aug 20, 2026 |
| 71335-1898-6 | 180 TABLET, FILM COATED in 1 BOTTLE (71335-1898-6) | Aug 20, 2026 |
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