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

Is NDC 39822-0255-01 recalled?

Cyclophosphamide · 1 VIAL, SINGLE-DOSE in 1 CARTON (39822-0255-1) / 50 mL in 1 VIAL, SINGLE-DOSE

Yes — this exact package was recalled

1 FDA recall names the code 39822-0255-01 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
Cyclophosphamide
Strength
CYCLOPHOSPHAMIDE 1 g/50mL
Form
Injection, Powder, Lyophilized, for Solution · Intravenous, Oral
Labeler
XGen Pharmaceuticals DJB, Inc.
Type
Human Prescription Drug
Product code
39822-0255

Recalls naming this package

Class III · Low risk

Cyclophosphamide for Injection

Labeling: Incorrect or missing Package Insert: There is an error on the Package Insert (PI), section 2.3, Preparation, Handling, and Administration. The concentration of the reconstituted product is listed as '20 mg per vial.' This information should read: '20 mg per mL'.

Terminated Labeling / mix-up X-Gen Pharmaceuticals Inc. NDC 39822-0255-01 D-0434-2024

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