NDC 52959-352

Lansoprazole 30 mg capsule, delayed release

On the label: H.J. Harkins Co., Inc..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
H.J. Harkins Company, Inc.Grover Beach, California, United StatesMakes it, repackages it and relabels it Problems found, fixed voluntarilyMar 3, 2023 · 5 inspections

Product details

Generic drug
Lansoprazole: every company that makes it
Form
capsule, delayed release
Strength
30 mg
Approval
ANDA ANDA091269
On the market since
Jan 9, 2018
Package NDCs
52959-352-07 52959-352-14
Official label
DailyMed (National Library of Medicine), updated Mar 15, 2018

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