Lupin Limited
Pithampur, India · makes it and packages it
Serious problems, FDA action Last FDA inspection Jul 17, 2025. 6 inspections on record, 4 with serious problems.
NDC 70518-4397
Lisinopril 10 mg tablet
On the label: Remedyrepack Inc..
It's a repackaged product: Remedyrepack Inc. rebottles it from BluePoint Laboratories.'s NDC 68001-334.
Where the pills inside were made
Lupin Limited
Nagpur, India · makes it and packages it
Problems found, fixed voluntarily Last FDA inspection Jul 11, 2023. 4 inspections on record.
Recalls
- Jul 17, 2020 · Class II · Terminated
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
Product details
- Generic drug
- Lisinopril: see every company that makes it
- Form
- tablet, oral
- Strength
- 10 mg
- Approval
- ANDA ANDA077321
- On the market since
- Jul 23, 2025
- Package NDCs
70518-4397-0- Official label
- DailyMed (National Library of Medicine), updated Oct 28, 2026
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