NDC 68071-2999
Finasteride 5 mg tablet, film coated
On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Ascend Laboratories, LLC's NDC 67877-288.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Alkem Laboratories Limited | Baddi Solan, India | Makes it, tests it and packages it | Problems found, fixed voluntarilyMar 27, 2024 · 9 inspections |
Repackaging site
- NuCare Pharmaceuticals,Inc., Orange, CA, United States · relabels it
Product details
- Generic drug
- Finasteride: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 5 mg
- Approval
- ANDA ANDA204304
- On the market since
- Jan 5, 2017
- Package NDCs
68071-2999-9- Official label
- DailyMed (National Library of Medicine), updated Feb 4, 2025
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?