NDC 68788-8749
Finasteride 5 mg tablet, film coated
On the label: Preferred Pharmaceuticals, Inc... It's repackaged: Preferred Pharmaceuticals, 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 |
Repackaging site
- Preferred Pharmaceuticals Inc., Anaheim, CA, United States · repackages it
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
- Oct 11, 2024
- Package NDCs
68788-8749-168788-8749-368788-8749-668788-8749-9- Official label
- DailyMed (National Library of Medicine), updated Jan 19, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?