NDC 67046-1041
Lisinopril 10 mg tablet
On the label: Coupler LLC. It's repackaged: Coupler LLC rebottles it from BluePoint Laboratories.'s NDC 68001-334.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Lupin Limited | Pithampur, India | Makes it and packages it | Serious problems, FDA actionJul 17, 2025 · 6 inspections, 4 with FDA action |
| Lupin Limited | Nagpur, India | Makes it and packages it | Problems found, fixed voluntarilyJul 11, 2023 · 4 inspections |
Repackaging site
- Coupler LLC, West Chester, PA, United States · repackages it
Recalls
- Jul 17, 2020 · Class II · Lupin Pharmaceuticals Inc.
Presence of Foreign Tablets/Capsules: Lisinopril Tablets USP, 20mg found in a 1000 count bottle of Lisinopril Tablets USP, 10mg
Lots: Lot # Q000232, exp. date 01/2022
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Lisinopril: every company that makes it
- Form
- tablet
- Strength
- 10 mg
- Approval
- ANDA ANDA077321
- On the market since
- Nov 11, 2024
- Package NDCs
67046-1041-3- Official label
- DailyMed (National Library of Medicine), updated Nov 11, 2024
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