Class I ยท High risk
Acetaminophen Extra Strength Tablets
Labeling: Label Mix-Up: Some bottles of Acetaminophen Extra Strength 500 mg tablets were incorrectly labeled with the drug facts label for Aspirin 81 mg tablets.
National Drug Code
Is NDC 50090-5313-02 recalled?
Acetaminophen · 100 TABLET in 1 BOTTLE (50090-5313-2)
Yes — this exact package was recalled
1 FDA recall names the code 50090-5313-02 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
- Strength
- ACETAMINOPHEN 500 mg/1
- Form
- Tablet · Oral
- Labeler
- A-S Medication Solutions
- Type
- Human OTC Drug
- Product code
- 50090-5313
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
- 50090-1494 Metformin Hydrochloride 1
- 50090-5350 Acetaminophen 1
- 50090-5510 Cetirizine 1
Free recall alerts
Know the day your medication is recalled
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