Drugplain

NDC 55111-784-05

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 Dr. Reddy's Laboratories Limited.

Key Facts

Brand Name
Fexofenadine hydrochloride
Generic Name
Fexofenadine hydrochloride
NDC Code (Package)
55111-784-05
NDC Code (Product)
55111-784
Manufacturer
Dr. Reddy's Laboratories Limited
Strength
180 mg/1
Dosage Form
TABLET
Route
ORAL
Marketing Status
Application #
ANDA076502
Marketing Start
01/03/2011

Recall History

No Recall History

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