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

Is NDC 24385-0998-74 recalled?

good neighbor pharmacy all day allergy · 14 BLISTER PACK in 1 CARTON (24385-998-74) / 1 TABLET, FILM COATED in 1 BLISTER PACK

Yes — this exact package was recalled

1 FDA recall names the code 24385-0998-74 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
Cetirizine Hydrochloride
Strength
CETIRIZINE HYDROCHLORIDE 10 mg/1
Form
Tablet, Film Coated · Oral
Labeler
Amerisource Bergen
Type
Human OTC Drug
Product code
24385-0998

Recalls naming this package

Class III · Low risk

Cetirizine HCl 10 mg Tablet

Failed Impurity/Degradations Specifications; impurity identified as cetirizine monosaccharide ester

Terminated Impurity / degradation Perrigo Company PLC NDC 41163-458-66 D-0525-2016

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