Class II · Moderate risk
Acetaminophen and Ibuprofen
CGMP Deviations
National Drug Code
Is NDC 72657-0157-74 recalled?
Acetaminophen, Ibuprofen · 1 BOTTLE in 1 CARTON (72657-157-74) / 144 TABLET, FILM COATED in 1 BOTTLE
Yes — this exact package was recalled
1 FDA recall names the code 72657-0157-74 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, Ibuprofen
- Strength
- IBUPROFEN 125 mg/1; ACETAMINOPHEN 250 mg/1
- Form
- Tablet, Film Coated · Oral
- Labeler
- Glenmark Therapeutics INC., USA
- Type
- Human OTC Drug
- Product code
- 72657-0157
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
- 72657-0113 Famotidine 1
- 72657-0129 Cetirizine HCl 1
Free recall alerts
Know the day your medication is recalled
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