NDC 31722-525 – Finasteride
Finasteride 5 mg/1 · Tablet, Film Coated · Oral
Product NDC31722-525
Product details
- Brand name
- Finasteride
- Generic name
- Finasteride
- Labeler
- Camber Pharmaceuticals, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA090061
- Marketed since
- June 13, 2015
- Listing expires
- December 31, 2026
- Pharmacologic class
- 5-alpha Reductase Inhibitor
Active ingredients
- Finasteride 5 mg/1
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 31722-525-01 | 100 TABLET, FILM COATED in 1 BOTTLE (31722-525-01) | Jun 13, 2015 |
| 31722-525-05 | 500 TABLET, FILM COATED in 1 BOTTLE (31722-525-05) | Jun 13, 2015 |
| 31722-525-10 | 1000 TABLET, FILM COATED in 1 BOTTLE (31722-525-10) | Jun 13, 2015 |
| 31722-525-30 | 12 BOTTLE in 1 CASE (31722-525-30) / 30 TABLET, FILM COATED in 1 BOTTLE | Jun 13, 2015 |
| 31722-525-90 | 12 BOTTLE in 1 CASE (31722-525-90) / 90 TABLET, FILM COATED in 1 BOTTLE | Jun 13, 2015 |
Recalls mentioning this NDC
- D-0453-2017 Feb 8, 2017 · Class III
Failed Tablet/Capsule Specification: Tablets were found to be twice the thickness in one lot of product.
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