NDC 65219-385
Pantoprazole Sodium 40 mg per 10 mL injection, powder, lyophilized, for solution
On the label: Fresenius Kabi USA, LLC.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Fresenius Kabi USA, LLC | Melrose Park, IL, United States | Makes it and tests it | Problems found, fixed voluntarilyAug 24, 2023 · 13 inspections, 2 with FDA action |
Product details
- Generic drug
- Pantoprazole: every company that makes it
- Form
- injection, powder, lyophilized, for solution, intravenous
- Strength
- 40 mg per 10 mL
- Approval
- ANDA ANDA216021
- On the market since
- Aug 1, 2024
- Package NDCs
65219-385-0165219-385-10- Official label
- DailyMed (National Library of Medicine), updated Dec 31, 2024
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