NDC 10544-232
Glyburide 2.5 mg tablet
On the label: Blenheim Pharmacal, Inc.. It's repackaged: Blenheim Pharmacal, Inc. rebottles it from Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.'s NDC 23155-057.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| USV Private Limited | Daman, India | Makes it | Serious problems, FDA actionApr 17, 2026 · 8 inspections, 3 with FDA action |
| USV Private Limited | Ratnagiri, India | Makes the active ingredient | Problems found, fixed voluntarilySep 12, 2025 · 6 inspections |
Repackaging site
- Blenheim Pharmacal, Inc., North Blenheim, New York, United States · repackages it
Product details
- Generic drug
- Glyburide: every company that makes it
- Form
- tablet
- Strength
- 2.5 mg
- Approval
- ANDA ANDA090937
- On the market since
- Nov 15, 2013
- Package NDCs
10544-232-30- Official label
- DailyMed (National Library of Medicine), updated Mar 18, 2015
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?