NDC 67046-1519
Pravastatin Sodium 20 mg tablet
On the label: Coupler LLC. It's repackaged: Coupler LLC rebottles it from Cipla USA., Inc.'s NDC 69097-789.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Glenmark Pharmaceuticals Limited | Dhar, India | Makes it, tests it, packages it and labels it | Serious problems, FDA actionFeb 14, 2025 · 8 inspections, 1 with FDA action |
Repackaging site
- Coupler LLC, West Chester, PA, United States · repackages it
Product details
- Generic drug
- Pravastatin: every company that makes it
- Form
- tablet, oral
- Strength
- 20 mg
- Approval
- ANDA ANDA077987
- On the market since
- Feb 13, 2025
- Package NDCs
67046-1519-3- Official label
- DailyMed (National Library of Medicine), updated Feb 13, 2025
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