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

Is NDC 0363-0374-04 recalled?

migraine relief

Yes — this exact package was recalled

1 FDA recall names the code 0363-0374-04 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
Acetaminophen, Aspirin, Caffeine
Strength
ACETAMINOPHEN 250 mg/1; ASPIRIN 250 mg/1; CAFFEINE 65 mg/1
Form
Tablet, Film Coated · Oral
Labeler
Walgreen Company
Type
Human OTC Drug
Product code
0363-0374

Recalls naming this package

Class III · Low risk

Nicotine Polacrilex Lozenge

Failed Dissolution Specifications and Failed Tablet Specifications: High 30 minute dissolution test and presence of broken lozenges.

Terminated Dissolution failure Perrigo Holland Inc D-1558-2014

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