Class III · Low risk
Protonix I.V.
Subpotent Drug: Out of Specification (OOS) for potency at the 6-month stability time point.
National Drug Code
Is NDC 0008-4001-25 recalled?
Protonix I.V. · 25 CARTON in 1 PACKAGE (0008-4001-25) / 1 VIAL in 1 CARTON (0008-4001-01) / 10 mL in 1 VIAL
Yes — this exact package was recalled
1 FDA recall names the code 0008-4001-25 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.
- Active ingredient
- Pantoprazole Sodium
- Strength
- PANTOPRAZOLE SODIUM 40 mg/10mL
- Form
- Injection, Powder, for Solution · Intravenous
- Labeler
- Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.
- Type
- Human Prescription Drug
- Product code
- 0008-4001
Recalls naming this package
Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.
Other recalled products from this labeler
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