Class II · Moderate risk
Fexofenadine Hydrochloride Tablets
CGMP Deviations: Microbial contamination was reported in stagnant water in the duct of the manufacturing equipment.
National Drug Code
Is NDC 51660-0998-55 recalled?
Fexofenadine Hydrochloride · 1 BOTTLE in 1 CARTON (51660-998-55) / 150 TABLET, FILM COATED in 1 BOTTLE
Yes — this exact package was recalled
1 FDA recall names the code 51660-0998-55 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
- Ohm Laboratories INC.
- Type
- Human OTC Drug
- Product code
- 51660-0998
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
- 51660-0527 Allergy Relief 1
Free recall alerts
Know the day your medication is recalled
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