NDC 85509-1636
Pantoprazole Sodium 20 mg tablet, delayed release
On the label: Phoenix RX LLC. It's repackaged: Phoenix RX LLC rebottles it from Amneal Pharmaceuticals's NDC 65162-636.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Amneal Pharmaceuticals Private Limited | Ahmedabad, India | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyJan 24, 2025 · 9 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 ANDA205119
- On the market since
- Jun 20, 2016
- Package NDCs
85509-1636-385509-1636-685509-1636-9- Official label
- DailyMed (National Library of Medicine), updated Nov 20, 2025
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