NDC 76420-668
Pantoprazole Sodium 20 mg tablet, delayed release
On the label: Asclemed USA, Inc.. It's repackaged: Asclemed USA, Inc. rebottles it from XLCare Pharmaceuticals, Inc.'s NDC 72865-229.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Evaric Pharmaceuticals Inc | Hauppauge, NY, United States | Makes it and tests it | Problems found, fixed voluntarilyMay 16, 2025 · 3 inspections |
Repackaging site
- Asclemed USA Inc. dba Enovachem, Torrance, CA, United States · repackages it and relabels it
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
76420-668-1076420-668-3076420-668-6076420-668-90- Official label
- DailyMed (National Library of Medicine), updated Feb 14, 2024
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