NDC 70332-300
Pantoprazole Sodium 40 mg tablet, delayed release
On the label: Fusion Pharmaceuticals LLC. It's repackaged: Fusion Pharmaceuticals LLC rebottles it from Amneal Pharmaceuticals's NDC 65162-637.
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
- California Pharmaceuticals LLC, Camarillo, California, United States · repackages it
Product details
- Generic drug
- Pantoprazole: every company that makes it
- Form
- tablet, delayed release
- Strength
- 40 mg
- Approval
- ANDA ANDA205119
- On the market since
- Jul 1, 2017
- Package NDCs
70332-300-0170332-300-02- Official label
- DailyMed (National Library of Medicine), updated Aug 4, 2017
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