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

Is NDC 63323-0417-10 recalled?

Cisatracurium · 10 VIAL in 1 CARTON (63323-417-10) / 10 mL in 1 VIAL (63323-417-01)

Yes — this exact package was recalled

1 FDA recall names the code 63323-0417-10 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
Cisatracurium Besylate
Strength
CISATRACURIUM BESYLATE 2 mg/mL
Form
Injection, Solution · Intravenous
Labeler
Fresenius Kabi USA, LLC
Type
Human Prescription Drug
Product code
63323-0417

Recalls naming this package

Class II · Moderate risk

Cisatracurium Besylate Injection

Incorrect/ Undeclared Excipient: Firm is recalling product due to an incorrect statement of Preservative free on the individual carton label. The vial label and outer carton label contain the correct statement of 0.9% benzyl alcohol added as a preservative.

Terminated Chemical / undeclared Fresenius Kabi USA, LLC NDC 63323-417-10 D-0819-2016

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