NDC 82009-061 – Finasteride
Finasteride 5 mg/1 · Tablet, Film Coated · Oral
Product NDC82009-061
Product details
- Brand name
- Finasteride
- Generic name
- Finasteride
- Labeler
- QUALLENT PHARMACEUTICALS HEALTH LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA078341
- Marketed since
- November 21, 2022
- Listing expires
- December 31, 2027
- Pharmacologic class
- 5-alpha Reductase Inhibitor
Active ingredients
- Finasteride 5 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 82009-061-05 | 500 TABLET, FILM COATED in 1 BOTTLE (82009-061-05) | Nov 21, 2022 |
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