Drugplain

NDC 68016-995-45

Fexofenadine Hydrochloride 180 mg/1

Fexofenadine hydrochloride · TABLET

No Recall History

Fexofenadine Hydrochloride is a tablet containing fexofenadine hydrochloride at a strength of 180 mg/1. Manufactured by Chain Drug Consortium, LLC.

Key Facts

Brand Name
Fexofenadine Hydrochloride
Generic Name
Fexofenadine hydrochloride
NDC Code (Package)
68016-995-45
NDC Code (Product)
68016-995
Manufacturer
Chain Drug Consortium, LLC
Strength
180 mg/1
Dosage Form
TABLET
Route
ORAL
Marketing Status
Application #
ANDA076502
Marketing Start
04/01/2014

Recall History

No Recall History

Not medical advice. This information is for reference only. Always consult your doctor or pharmacist.