NDCFind

Fexofenadine Hydrochloride 68210-4090-01

Package NDC

68210-4090-01

Product NDC: 68210-4090

Manufacturer
Spirit Pharmaceuticals Llc
Dosage Form
Tablet, Film Coated
Route
Oral
Product Type
Human Otc Drug
Marketing Start
July 2, 2020
Listing Expires
December 31, 2026
Application
ANDA204507

Active Ingredients

IngredientStrength
Fexofenadine Hydrochloride180 mg/1

Drug Class

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

Selected Package

68210-4090-01Selected

100 TABLET, FILM COATED in 1 PACKAGE (68210-4090-1)