NDC 76420-669

Pantoprazole Sodium 40 mg tablet, delayed release

On the label: Asclemed USA, Inc.. It's repackaged: Asclemed USA, Inc. rebottles it from XLCare Pharmaceuticals, Inc.'s NDC 72865-230.

United States: 1

Where the pills inside were made

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

Repackaging site

Product details

Generic drug
Pantoprazole: every company that makes it
Form
tablet, delayed release, oral
Strength
40 mg
Approval
ANDA ANDA202882
On the market since
May 1, 2022
Package NDCs
76420-669-10 76420-669-30 76420-669-60 76420-669-90
Official label
DailyMed (National Library of Medicine), updated Feb 14, 2024

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