Class II · Moderate risk
Pantoprazole Sodium for Injection 40mg per vial
Lack of Assurance of Sterility: Powder discoloration due to small crack in some vials.
National Drug Code
Is NDC 71839-0122-01 recalled?
Pantoprazole sodium · 1 VIAL in 1 CARTON (71839-122-01) / 10 mL in 1 VIAL
Yes — this exact package was recalled
1 FDA recall names the code 71839-0122-01 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
- BE Pharmaceuticals Inc.
- Type
- Human Prescription Drug
- Product code
- 71839-0122
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
- 71839-0104 fosaprepitant 1
Free recall alerts
Know the day your medication is recalled
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