Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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National Drug Code

Is NDC 0143-9850-01 recalled?

Methylprednisolone Sodium Succinate · 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, MULTI-DOSE (0143-9850-01)

Yes — this exact package was recalled

1 FDA recall names the code 0143-9850-01 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
Methylprednisolone Sodium Succinate
Strength
METHYLPREDNISOLONE SODIUM SUCCINATE 500 mg/1
Form
Injection, Powder, for Solution · Intramuscular, Intravenous
Labeler
Hikma Pharmaceuticals USA Inc.
Type
Human Prescription Drug
Product code
0143-9850

Recalls naming this package

Class III · Low risk

methylPREDNISolone Sodium Succinate For Injection

Labeling: Incorrect Instructions: Vial label incorrectly instructs healthcare professional to reconstitute product with 16 mL rather than the correct volume of 8 mL of Bacteriostatic Water for Injection with Benzyl Alcohol.

Terminated Labeling / mix-up Hikma Pharmaceuticals USA Inc. NDC 0143-9850-01 D-0801-2020

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