NDC 68071-4808
Finasteride 1 mg tablet, film coated
On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Aurobindo Pharma Limited's NDC 65862-927.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurobindo Pharma Limited | Medchal, India | Makes it and tests it | Problems found, fixed voluntarilyJul 21, 2023 · 13 inspections, 1 with FDA action |
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
- 1 mg
- Approval
- ANDA ANDA203687
- On the market since
- Sep 20, 2014
- Package NDCs
68071-4808-3- Official label
- DailyMed (National Library of Medicine), updated Jun 14, 2024
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