Class II · Moderate risk
Ibuprofen 800mg
Failed Impurities/Degradation Specifications: Product failed impurity specifications at the 18-month stability testing.
National Drug Code
Is NDC 61919-0621 recalled?
Ibuprofen 800mg
This product was recalled — in other package sizes
No FDA recall names your exact package code, but 1 recall cover the same product (61919-0621) in a different bottle or carton size. Worth checking with your pharmacist.
1 of these recalls is still ongoing.
This code is not in the current FDA NDC directory — usual for a product that has since been discontinued or repackaged. The details below come from the recall notices themselves.
Recalls of this product
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
- 61919-0482 See recall 2
- 61919-0775 See recall 2
- 61919-0009 See recall 1
- 61919-0040 See recall 1
- 61919-0250 See recall 1
- 61919-0339 See recall 1
Free recall alerts
Know the day your medication is recalled
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