NDC 47335-714 – Finasteride
Finasteride 1 mg/1 · Tablet, Film Coated · Oral
Product NDC47335-714
Product details
- Brand name
- Finasteride
- Generic name
- Finasteride
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA090508
- Marketed since
- November 23, 2022
- Listing expires
- December 31, 2026
- Pharmacologic class
- 5-alpha Reductase Inhibitor
Active ingredients
- Finasteride 1 mg/1
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 47335-714-08 | 100 TABLET, FILM COATED in 1 BOTTLE (47335-714-08) | Nov 23, 2022 |
| 47335-714-18 | 1000 TABLET, FILM COATED in 1 BOTTLE (47335-714-18) | Nov 23, 2022 |
| 47335-714-81 | 90 TABLET, FILM COATED in 1 BOTTLE (47335-714-81) | Nov 23, 2022 |
| 47335-714-83 | 30 TABLET, FILM COATED in 1 BOTTLE (47335-714-83) | Nov 23, 2022 |
| 47335-714-88 | 100 TABLET, FILM COATED in 1 BOTTLE (47335-714-88) | Nov 23, 2022 |
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