NDC 68071-3776

Pantoprazole 20 mg tablet, delayed release

On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Northstar Rx LLC.'s NDC 72603-177.

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
Pantoprazole: every company that makes it
Form
tablet, delayed release, oral
Strength
20 mg
Approval
ANDA ANDA077619
On the market since
Dec 15, 2023
Package NDCs
68071-3776-3 68071-3776-6
Official label
DailyMed (National Library of Medicine), updated Jan 29, 2025

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