Class III · Low risk
Allergy & Congestion Fexofenadine HCl 60 mg & Pseudoephedrine HCl…
Failed dissolution specifications
National Drug Code
Is NDC 11822-7388-05 recalled?
Allergy and Congestion · 4 BLISTER PACK in 1 CARTON (11822-7388-5) / 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Yes — this exact package was recalled
1 FDA recall names the code 11822-7388-05 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.
- Active ingredient
- Fexofenadine HCl and Pseudoephedrine HCI
- Strength
- FEXOFENADINE HYDROCHLORIDE 60 mg/1; PSEUDOEPHEDRINE…
- Form
- Tablet, Extended Release · Oral
- Labeler
- Rite Aid Corporation
- Type
- Human OTC Drug
- Product code
- 11822-7388
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
- 11822-0571 See recall 1
Free recall alerts
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