NDC 67046-426
Lisinopril 10 mg tablet
On the label: Coupler Enterprises Inc.. It's repackaged: Coupler Enterprises Inc. rebottles it from Ranbaxy Laboratories Inc.'s NDC 63304-533.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Matrix Pharmacorp Private Limited | Hyderabad, India | Makes the active ingredient | Problems found, fixed voluntarilyNov 28, 2025 · 6 inspections |
| Ohm Laboratories Inc. | North Brunswick, NJ, United States | Makes it and packages it | No problems foundOct 31, 2024 · 22 inspections |
| Ranbaxy laboratories Limited Toansa | Location not on file | Makes the active ingredient | Not inspected on record |
| Zhejiang Huahai Pharmaceutical Co., Ltd. | Linhai, China | Makes it and makes the active ingredient | Serious problems, FDA actionApr 24, 2026 · 8 inspections, 3 with FDA action |
| Ohm Laboratories Inc. | New Brunswick, NJ, United States | Packages it | No problems foundOct 31, 2024 · 22 inspections |
Product details
- Generic drug
- Lisinopril: every company that makes it
- Form
- tablet
- Strength
- 10 mg
- Approval
- ANDA ANDA075944
- On the market since
- Jul 2, 2002
- Package NDCs
67046-426-30- Official label
- DailyMed (National Library of Medicine), updated Oct 12, 2009
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