NDC 70518-3616
Finasteride 5 mg tablet, film coated
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Aurobindo Pharma Limited's NDC 65862-149.
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
- 5 mg
- Approval
- ANDA ANDA078341
- On the market since
- Jan 18, 2023
- Package NDCs
70518-3616-070518-3616-170518-3616-270518-3616-370518-3616-470518-3616-5- Official label
- DailyMed (National Library of Medicine), updated Oct 14, 2026
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