Class II · Moderate risk
allergy relief
Failed Impurities/Degradation Specifications
National Drug Code
Is NDC 79481-0847-02 recalled?
allergy relief · 1 BOTTLE in 1 CARTON (79481-0847-2) / 45 TABLET, FILM COATED in 1 BOTTLE
Yes — this exact package was recalled
1 FDA recall names the code 79481-0847-02 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 hydrochloride
- Strength
- FEXOFENADINE HYDROCHLORIDE 180 mg/1
- Form
- Tablet, Film Coated · Oral
- Labeler
- Meijer, Inc.
- Type
- Human OTC Drug
- Product code
- 79481-0847
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
- 79481-0034 Magnesium Citrate 1
Free recall alerts
Know the day your medication is recalled
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