NDCFind

Fexofenadine Hydrochloride 10202-0229-66

Package NDC

10202-0229-66

Product NDC: 10202-0229

Manufacturer
7-Eleven
Dosage Form
Tablet, Film Coated
Route
Oral
Product Type
Human Otc Drug
Marketing Start
January 15, 2015
Listing Expires
December 31, 2026
Application
ANDA202039

Active Ingredients

IngredientStrength
Fexofenadine Hydrochloride180 mg/1

Drug Class

Histamine H1 Receptor Antagonists [MoA]Histamine-1 Receptor Antagonist [EPC]

Selected Package

10202-0229-66Selected

1 BLISTER PACK in 1 CARTON (10202-229-66) / 10 TABLET, FILM COATED in 1 BLISTER PACK