NDC 59651-002

Omeprazole 20 mg capsule, delayed release

On the label: Aurobindo Pharma Limited.

India: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Aurobindo Pharma LimitedMahabubnagar, IndiaMakes it and tests it Problems found, fixed voluntarilyMay 10, 2022 · 7 inspections, 1 with FDA action

Product details

Generic drug
Omeprazole: every company that makes it
Form
capsule, delayed release, oral
Strength
20 mg
Approval
ANDA ANDA203270
On the market since
Aug 19, 2015
Package NDCs
59651-002-01 59651-002-03 59651-002-05 59651-002-10 59651-002-30 59651-002-78 59651-002-90 59651-002-99
Official label
DailyMed (National Library of Medicine), updated Jun 17, 2024

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