NDC 85509-1332
Pantoprazole 20 mg tablet, delayed release
On the label: Phoenix RX LLC. It's repackaged: Phoenix RX LLC rebottles it from Dr.Reddy's Laboratories Ltd.'s NDC 55111-332.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Dr. Reddy's Laboratories Limited | Medchal-Malkajgiri, India | Makes it and tests it | Problems found, fixed voluntarilyOct 27, 2023 · 8 inspections |
Repackaging site
- Phoenix RX LLC, Hatboro, PA, 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 ANDA077619
- On the market since
- Jan 19, 2011
- Package NDCs
85509-1332-385509-1332-685509-1332-9- Official label
- DailyMed (National Library of Medicine), updated Nov 19, 2025
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