NDC 16729-089 – Finasteride
Finasteride 1 mg/1 · Tablet, Film Coated · Oral
Product NDC16729-089
Product details
- Brand name
- Finasteride
- Generic name
- Finasteride
- Labeler
- Accord Healthcare, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA091643
- Marketed since
- November 8, 2013
- Listing expires
- December 31, 2026
- Pharmacologic class
- 5-alpha Reductase Inhibitor
Active ingredients
- Finasteride 1 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 16729-089-10 | 30 TABLET, FILM COATED in 1 BOTTLE (16729-089-10) | Nov 8, 2013 |
| 16729-089-15 | 90 TABLET, FILM COATED in 1 BOTTLE (16729-089-15) | Jan 17, 2014 |
Recalls mentioning this NDC
- D-0390-2023 Mar 8, 2023 · Class II
CGMP Deviations: recalling drug products following an FDA inspection.
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