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

Is NDC 72485-0203-30 recalled?

Imatinib mesylate 400 mg · 30 TABLET, FILM COATED in 1 BOTTLE (72485-203-30)

Yes — this exact package was recalled

1 FDA recall names the code 72485-0203-30 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
imatinib mesylate
Strength
IMATINIB MESYLATE 400 mg/1
Form
Tablet, Film Coated · Oral
Labeler
Armas Pharmaceuticals Inc.
Type
Human Prescription Drug
Product code
72485-0203

Recalls naming this package

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