NDC 53808-1123
Pantoprazole Sodium 20 mg tablet, delayed release
On the label: State of Florida DOH Central Pharmacy. It's repackaged: State of Florida DOH Central Pharmacy 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 |
Repackaging site
- State of Florida DOH Central Pharmacy, Location not on file · repackages it
Product details
- Generic drug
- Pantoprazole: every company that makes it
- Form
- tablet, delayed release
- Strength
- 20 mg
- Approval
- ANDA ANDA202038
- On the market since
- Aug 21, 2017
- Package NDCs
53808-1123-1- Official label
- DailyMed (National Library of Medicine), updated Jan 23, 2019
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