NDC 68382-412

Omeprazole 20 mg capsule, delayed release

On the label: Zydus Pharmaceuticals (USA) Inc..

Where it's made

Zydus Lifesciences Limited

Ahmedabad, India · makes it and tests it

Problems found, fixed voluntarily Last FDA inspection Aug 5, 2022. 10 inspections on record, 3 with serious problems.

Product details

Generic drug

Omeprazole: see every company that makes it

Form

capsule, delayed release, oral

Strength

20 mg

Approval

ANDA ANDA091352

On the market since

Nov 23, 2012

Package NDCs

68382-412-01 68382-412-05 68382-412-06 68382-412-10 68382-412-16

Official label

DailyMed (National Library of Medicine), updated May 11, 2023

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