Fexofenadine

FDA Drug Profile — Fexofenadine

Fexofenadine is listed in the FDA National Drug Code directory with 1 NDC code, marketed under brand name including Fexofenadine. Available dosage form: tablet.

Drug Details

Generic Name
Fexofenadine
Brand Names
Fexofenadine
Application Number
ANDA219032
Sponsor
YYBA Corp
NDC Codes
1
Dosage Forms
TABLET
Routes
ORAL
Active Ingredients
FEXOFENADINE HYDROCHLORIDE

Indications and Usage

Uses temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: • runny nose • itchy, watery eyes • sneezing • itching of the nose or throat

Warnings

Warnings Do not use if you have ever had an allergic reaction to this product or any of its ingredients. Ask a doctor before use if you have kidney disease. Your doctor should determine if you need a different dose. When using this product • do not take more than directed • do not take at the same time as aluminum or magnesium antacids • do not take with fruit juices (see Directions) Stop use and ask a doctor if an allergic reaction to this product occurs. Seek medical help right away. If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222).