Class I · High risk
Pantoprazole Sodium for Injection
Presence of Particulate Matter: One vial from a lot of Pantoprazole Sodium for Injection (40 mg) contained a piece of glass
National Drug Code
Is NDC 55150-0202-00 recalled?
Pantoprazole Sodium
Yes — this exact package was recalled
2 FDA recalls name the code 55150-0202-00 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/1
- Form
- Injection, Powder, for Solution · Intravenous
- Labeler
- Eugia US LLC
- Type
- Human Prescription Drug
- Product code
- 55150-0202
Recalls naming this package
Class III · Low risk
Pantoprazole Sodium for Injection
Discoloration: Some vials were found to contain powder with a yellowish-brownish appearance.
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
- 55150-0120 Piperacillin and Tazobactam 2
- 55150-0183 Nicardipine Hydrochloride 2
- 55150-0242 Linezolid 2
- 55150-0243 Levofloxacin 2
- 55150-0306 Progesterone 2
- 55150-0113 Ampicillin 1
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