NDC 68071-3733

Omeprazole 20 mg capsule, delayed release

On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Dr.Reddy's Laboratories Ltd.'s NDC 55111-644.

India: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Dr. Reddy's Laboratories LimitedMedchal-Malkajgiri, IndiaMakes it and tests it Problems found, fixed voluntarilyOct 27, 2023 · 8 inspections

Repackaging site

Product details

Generic drug
Omeprazole: every company that makes it
Form
capsule, delayed release, oral
Strength
20 mg
Approval
ANDA ANDA078490
On the market since
Mar 1, 2014
Package NDCs
68071-3733-2 68071-3733-3 68071-3733-6 68071-3733-9
Official label
DailyMed (National Library of Medicine), updated Sep 29, 2025

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