NDC 68071-3895
Pravastatin sodium 20 mg tablet
On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Aurobindo Pharma Limited's NDC 84386-032.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Teva Czech Industries s.r.o. | Opava, Czech Republic | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyAug 30, 2024 · 8 inspections |
| Teva Pharmaceutical Industries Ltd. | Kfar Saba, Israel | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyMay 23, 2023 · 6 inspections |
Repackaging site
- NuCare Pharmaceuticals,Inc., Orange, CA, United States · repackages it
Product details
- Generic drug
- Pravastatin: every company that makes it
- Form
- tablet, oral
- Strength
- 20 mg
- Approval
- ANDA ANDA076056
- On the market since
- Feb 27, 2025
- Package NDCs
68071-3895-9- Official label
- DailyMed (National Library of Medicine), updated Oct 27, 2025
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?