PlainRecalls
FDA Drug Moderate Class II Terminated

Allergy (Fexofenadine Hydrochloride) Tablets USP, 180 mg, 30-count bottles, Distributed by: Aurohealth LLC, 2572 Brunswick Pike, Lawrenceville, NJ 08648; NDC 58602-820-09.

Reported: September 25, 2019 Initiated: August 23, 2019 #D-1872-2019

Product Description

Allergy (Fexofenadine Hydrochloride) Tablets USP, 180 mg, 30-count bottles, Distributed by: Aurohealth LLC, 2572 Brunswick Pike, Lawrenceville, NJ 08648; NDC 58602-820-09.

Reason for Recall

Failed Impurities/Degradation Specifications

Details

Recalling Firm
Aurolife Pharma, LLC
Units Affected
240 bottles
Distribution
Nationwide in the USA
Location
Dayton, NJ

Frequently Asked Questions

What product was recalled?
Allergy (Fexofenadine Hydrochloride) Tablets USP, 180 mg, 30-count bottles, Distributed by: Aurohealth LLC, 2572 Brunswick Pike, Lawrenceville, NJ 08648; NDC 58602-820-09.. Recalled by Aurolife Pharma, LLC. Units affected: 240 bottles.
Why was this product recalled?
Failed Impurities/Degradation Specifications
Which agency issued this recall?
This recall was issued by the FDA Drug on September 25, 2019. Severity: Moderate. Recall number: D-1872-2019.