NDC 65862-559
Pantoprazole Sodium 20 mg tablet, delayed release
On the label: Aurobindo Pharma Limited.
Where it's 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
- Sep 28, 2012
- Package NDCs
65862-559-1065862-559-9065862-559-99- Official label
- DailyMed (National Library of Medicine), updated Feb 6, 2026
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