NDCFind

Fexofenadine Hydrochloride 73629-0008-03

Package NDC

73629-0008-03

Product NDC: 73629-0008

Manufacturer
Amz789 Llc
Dosage Form
Tablet, Film Coated
Route
Oral
Product Type
Human Otc Drug
Marketing Start
July 27, 2024
Listing Expires
December 31, 2027
Application
ANDA211075

Active Ingredients

IngredientStrength
Fexofenadine Hydrochloride180 mg/1

Drug Class

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

Selected Package

73629-0008-03Selected

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (73629-008-03)