NDC 68788-6881

Omeprazole 20 mg capsule, delayed release

On the label: Preferred Pharmaceuticals, Inc... It's repackaged: Preferred Pharmaceuticals, Inc.. rebottles it from Glenmark Pharmaceuticals Inc., USA's NDC 68462-396.

India: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Glenmark Pharmaceuticals LimitedGoa, IndiaMakes it and tests it Problems found, fixed voluntarilyJun 30, 2026 · 7 inspections, 1 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 ANDA091672
On the market since
Jan 20, 2017
Package NDCs
68788-6881-1 68788-6881-2 68788-6881-3 68788-6881-4 68788-6881-6 68788-6881-8 68788-6881-9
Official label
DailyMed (National Library of Medicine), updated Sep 25, 2026

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