NDC 43063-983
Lovastatin 20 mg tablet
On the label: PD-Rx Pharmaceuticals, Inc.. It's repackaged: PD-Rx Pharmaceuticals, Inc. rebottles it from Carlsbad Technology, Inc.'s NDC 61442-142.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Carlsbad Technology, Inc. | Carlsbad, CA, United States | Makes it | Problems found, fixed voluntarilyJun 30, 2026 · 12 inspections |
Repackaging site
- PD-Rx Pharmaceuticals Inc., Oklahoma City, OK, United States · repackages it
Product details
- Generic drug
- Lovastatin: every company that makes it
- Form
- tablet, oral
- Strength
- 20 mg
- Approval
- ANDA ANDA075991
- On the market since
- Nov 25, 2002
- Package NDCs
43063-983-30- Official label
- DailyMed (National Library of Medicine), updated Mar 13, 2025
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