NDC 70518-4687
Finasteride 1 mg tablet, film coated
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Rising Pharma Holdings, Inc.'s NDC 57237-061.
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 |
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
- Jun 30, 2026
- Package NDCs
70518-4687-070518-4687-1- Official label
- DailyMed (National Library of Medicine), updated Jun 30, 2026
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