NDC 55150-202
Pantoprazole Sodium 40 mg injection, powder, for solution
On the label: AuroMedics Pharma LLC.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Eugia Pharma Specialities Limited | Sangareddy, India | Makes it, tests it and packages it | Serious problems, FDA actionFeb 6, 2026 · 7 inspections, 2 with FDA action |
Recalls
- Dec 4, 2017 · Class I · AuroMedics Pharma LLC
Presence of Particulate Matter: One vial from a lot of Pantoprazole Sodium for Injection (40 mg) contained a piece of glass
Lots: Lot # CPO170035 - Dec 16, 2016 · Class III · Aurobindo Pharma USA Inc
Discoloration: Some vials were found to contain powder with a yellowish-brownish appearance.
Lots: Lot #: CPO160028, Exp. June 2018
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Pantoprazole: every company that makes it
- Form
- injection, powder, for solution, intravenous
- Strength
- 40 mg
- Approval
- ANDA ANDA205675
- On the market since
- Mar 30, 2016
- Package NDCs
55150-202-0055150-202-1055150-202-25- Official label
- DailyMed (National Library of Medicine), updated Jul 9, 2026
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