NDC 50090-7019

Omeprazole 20 mg capsule, delayed release

On the label: A-S Medication Solutions. It's repackaged: A-S Medication Solutions rebottles it from Zydus Pharmaceuticals (USA) Inc.'s NDC 68382-412.

India: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Zydus Lifesciences LimitedAhmedabad, IndiaMakes it and tests it Problems found, fixed voluntarilyAug 5, 2022 · 10 inspections, 3 with FDA action

Repackaging site

Product details

Generic drug
Omeprazole: 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
50090-7019-0
Official label
DailyMed (National Library of Medicine), updated Jul 24, 2024

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