NDCFind

Fexofenadine Hcl 71205-0531

Product NDC

71205-0531
Manufacturer
Proficient Rx Lp
Dosage Form
Tablet
Route
Oral
Product Type
Human Otc Drug
Marketing Start
August 19, 2016
Listing Expires
December 31, 2026
Application
ANDA204097

Active Ingredients

IngredientStrength
Fexofenadine Hydrochloride180 mg/1

Drug Class

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

Packaging Options(6)

10 TABLET in 1 BOTTLE (71205-531-10)

15 TABLET in 1 BOTTLE (71205-531-15)

20 TABLET in 1 BOTTLE (71205-531-20)

30 TABLET in 1 BOTTLE (71205-531-30)

60 TABLET in 1 BOTTLE (71205-531-60)

90 TABLET in 1 BOTTLE (71205-531-90)