NDC 53808-0700
Lisinopril 10 mg tablet
On the label: State of Florida DOH Central Pharmacy. It's repackaged: State of Florida DOH Central Pharmacy rebottles it from Aurobindo Pharma Limited's NDC 65862-039.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Apl Healthcare Limited | Tirupati, India | Makes it and tests it | Problems found, fixed voluntarilyDec 17, 2025 · 5 inspections |
| Aurobindo Pharma Limited | Medchal, India | Makes it and tests it | Problems found, fixed voluntarilyJul 21, 2023 · 13 inspections, 1 with FDA action |
Recalls
- Apr 9, 2013 · Class III · Aurobindo Pharma USA Inc
Labeling: Label Error on Declared Strength: Incorrect strength on side display panel of label
Lots: Lot KP3012001-A Exp.12/13 Lot KP3012002-A Exp.12/13
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 ANDA077622
- On the market since
- Jul 1, 2009
- Package NDCs
53808-0700-1- Official label
- DailyMed (National Library of Medicine), updated Aug 19, 2010
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