NDC 72865-229

Pantoprazole Sodium 20 mg tablet, delayed release

On the label: XLCare Pharmaceuticals, Inc..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Evaric Pharmaceuticals IncHauppauge, NY, United StatesMakes it and tests it Problems found, fixed voluntarilyMay 16, 2025 · 3 inspections

Product details

Generic drug
Pantoprazole: every company that makes it
Form
tablet, delayed release, oral
Strength
20 mg
Approval
ANDA ANDA202882
On the market since
May 1, 2022
Package NDCs
72865-229-90
Official label
DailyMed (National Library of Medicine), updated Jan 17, 2023

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