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

Is NDC 0143-9702-01 recalled?

Irinotecan Hydrochloride · 2 mL in 1 VIAL, GLASS (0143-9702-01)

Yes — this exact package was recalled

1 FDA recall names the code 0143-9702-01 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
Irinotecan Hydrochloride
Strength
IRINOTECAN HYDROCHLORIDE 20 mg/mL
Form
Injection · Intravenous
Labeler
Hikma Pharmaceuticals USA Inc.
Type
Human Prescription Drug
Product code
0143-9702

Recalls naming this package

Class II · Moderate risk

Irinotecan Hydrochloride Injection

Superpotent Drug: a recent review of the USP revealed that an incorrect calculation was used to determine the amount of irinotecan to use in formulation which will result in an assay higher than the labeled claim.

Terminated Wrong potency / content West-Ward Pharmaceutical Corp. NDC 0143-9702-01 D-66447-001

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