NDC 10544-241
Lovastatin 20 mg tablet
On the label: Blenheim Pharmacal, Inc.. It's repackaged: Blenheim Pharmacal, 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
- Blenheim Pharmacal, Inc., North Blenheim, New York, United States · repackages it
Product details
- Generic drug
- Lovastatin: every company that makes it
- Form
- tablet
- Strength
- 20 mg
- Approval
- ANDA ANDA075991
- On the market since
- Oct 9, 2013
- Package NDCs
10544-241-30- Official label
- DailyMed (National Library of Medicine), updated Feb 20, 2015
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