NDC 85534-0061
Pantoprazole Sodium 40 mg tablet, delayed release
On the label: Hawaii Repack, Inc.. It's repackaged: Hawaii Repack, Inc. rebottles it from Aurobindo Pharma Limited's NDC 65862-560.
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
- 40 mg
- Approval
- ANDA ANDA202038
- On the market since
- Sep 28, 2012
- Package NDCs
85534-0061-085534-0061-185534-0061-285534-0061-385534-0061-485534-0061-5- Official label
- DailyMed (National Library of Medicine), updated Jun 26, 2026
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