FDAFDA · Food and drugs·Recall number D-1871-2019
Fexofenadine HCL Tablets USP, 180 mg, 500's BRITE STOCK; Manufactured for: Aurohealth LLC., 2572 Brunswick Pike, Lawrenceville, NJ 08648; Manufactured by: Aurolife Pharma LLC, Dayton, NJ 08810.
Published September 25, 2019 · Recall initiated: August 23, 2019
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Failed Impurities/Degradation Specifications
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Aurolife Pharma, LLC
- Distributor
- Nationwide in the USA
- Lot
- Lot #s:067180011A, 067180012A, Exp 04/21, 06718027B1, Exp 09/21
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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