Class II · Moderate risk
Rite Aid ALLERGY RELIEF Fexofenadine Hydrochloride tablets
Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
National Drug Code
Is NDC 11822-0571-05 recalled?
Rite Aid ALLERGY RELIEF Fexofenadine Hydrochloride tablets
Yes — this exact package was recalled
1 FDA recall names the code 11822-0571-05 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.
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 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
- 11822-0852 See recall 4
- 11822-4540 See recall 2
- 11822-4811 See recall 2
- 11822-0419 See recall 1
- 11822-0425 See recall 1
- 11822-0734 See recall 1
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