NDC 33358-211

Lisinopril 5 mg tablet

On the label: RxChange Co.. It's a repackaged product: RxChange Co. rebottles it from Lupin Pharmaceuticals, Inc.'s NDC 68180-512.

Where the pills inside were made

Lupin Limited

Salcette, India · makes it and packages it

Problems found, fixed voluntarily Last FDA inspection Nov 21, 2025. 9 inspections on record, 1 with serious problems.

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.

Lupin Limited

Nagpur, India · makes it and packages it

Problems found, fixed voluntarily Last FDA inspection Jul 11, 2023. 4 inspections on record.

Repackaging site

Recalls

Product details

Generic drug
Lisinopril: see every company that makes it
Form
tablet
Strength
5 mg
Approval
ANDA ANDA077321
On the market since
Nov 18, 2014
Package NDCs
33358-211-30
Official label
DailyMed (National Library of Medicine), updated Nov 19, 2014

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