NDC 67046-1494
Pregabalin 50 mg capsule
On the label: Coupler LLC. It's repackaged: Coupler LLC rebottles it from Aurobindo Pharma Limited's NDC 65862-759.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurobindo Pharma Limited | Mahabubnagar, India | Makes it and tests it | Problems found, fixed voluntarilyMay 10, 2022 · 7 inspections, 1 with FDA action |
Repackaging site
- Coupler LLC, West Chester, PA, United States · repackages it
Product details
- Generic drug
- Pregabalin: every company that makes it
- Form
- capsule, oral
- Strength
- 50 mg
- Approval
- ANDA ANDA205321
- On the market since
- Jan 28, 2025
- Package NDCs
67046-1494-3- Official label
- DailyMed (National Library of Medicine), updated Jan 28, 2025
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?