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

Is NDC 55305-0135-01 recalled?

AeroTab Pain Reliever · 25 PACKET in 1 BOX (55305-135-01) / 2 TABLET, FILM COATED in 1 PACKET

Yes — this exact package was recalled

1 FDA recall names the code 55305-0135-01 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.

1 of these recalls is still ongoing.

Active ingredient
Pain Reliever
Strength
ASPIRIN 500 mg/1; CAFFEINE 32.5 mg/1
Form
Tablet, Film Coated · Oral
Labeler
Aero Healthcare
Type
Human OTC Drug
Product code
55305-0135

Recalls naming this package

Class II ยท Moderate risk

Acetaminophen 500mg Caffeine 65mg caplets

Labeling: Label Mix-up. This issue affects the outer box labeling only. The box incorrectly states the ingredients Acetaminophen 500mg and Caffeine 65mg. The inner pouch correctly states the ingredients are Aspirin (NSAID)*500mg and Caffeine 32.5mg.

Ongoing Labeling / mix-up Aero Healthcare NDC 55305-135-01 D-0155-2026

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.