Class II · Moderate risk
Extra Strength Acetaminophen 500 MG Tablets
Discoloration: Brownish tablets
National Drug Code
Is NDC 0904-6730-60 recalled?
Acetaminophen · 100 TABLET in 1 BOTTLE (0904-6730-60)
Yes — this exact package was recalled
2 FDA recalls name the code 0904-6730-60 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
- Acetaminophen
- Strength
- ACETAMINOPHEN 500 mg/1
- Form
- Tablet · Oral
- Labeler
- Major Pharmaceuticals
- Type
- Human OTC Drug
- Product code
- 0904-6730
Recalls naming this package
Class II · Moderate risk
Major Extra Strength Acetaminophen Tablets
Presence of Foreign Tablets/Capsules: Complaint involving one Women's Prenatal dietary supplement tablet commingled in a bottle of Extra Strength Acetaminophen 500 mg contents 1000 count bottle.
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
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