NDC 53808-0701
Lisinopril 20 mg tablet
On the label: State of Florida DOH Central Pharmacy. It's repackaged: State of Florida DOH Central Pharmacy rebottles it from Ranbaxy Laboratories Inc.'s NDC 63304-534.
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
- 20 mg
- Approval
- ANDA ANDA075944
- On the market since
- Jul 1, 2009
- Package NDCs
53808-0701-1- Official label
- DailyMed (National Library of Medicine), updated Mar 8, 2010
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