NDC 70518-1788
Pantoprazole Sodium 20 mg tablet, delayed release
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Aurobindo Pharma Limited's NDC 65862-559.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurobindo Pharma Limited | Mahabubnagar, India | Makes it and tests it | Problems found, fixed voluntarilyMay 10, 2022 · 7 inspections, 1 with FDA action |
Product details
- Generic drug
- Pantoprazole: every company that makes it
- Form
- tablet, delayed release, oral
- Strength
- 20 mg
- Approval
- ANDA ANDA202038
- On the market since
- Jan 11, 2019
- Package NDCs
70518-1788-070518-1788-170518-1788-270518-1788-370518-1788-4- Official label
- DailyMed (National Library of Medicine), updated Jul 14, 2026
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