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

Is NDC 63323-0972-10 recalled?

Fosaprepitant · 1 VIAL, SINGLE-DOSE in 1 CARTON (63323-972-10) / 10 mL in 1 VIAL, SINGLE-DOSE

Yes — this exact package was recalled

1 FDA recall names the code 63323-0972-10 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
Fosaprepitant
Strength
FOSAPREPITANT DIMEGLUMINE 150 mg/5mL
Form
Injection, Powder, Lyophilized, for Solution · Intravenous
Labeler
Fresenius Kabi USA, LLC
Type
Human Prescription Drug
Product code
63323-0972

Recalls naming this package

Class III · Low risk

Fosaprepitant for Injection

Labeling Error: Label Error on Declared Strength: Carton label and product insert incorrectly states the quantity of the excipient edetate disodium (EDTA) as 5.4 mg / vial, rather than the actual amount of 18.8 mg / vial.

Terminated Labeling / mix-up Fresenius Kabi USA, LLC NDC 63323-972-10 D-1391-2020

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