NDCFind

Fexofenadine Hydrochloride 51660-0998-30

Package NDC

51660-0998-30

Product NDC: 51660-0998

Manufacturer
Ohm Laboratories Inc.
Dosage Form
Tablet, Film Coated
Route
Oral
Product Type
Human Otc Drug
Marketing Start
April 29, 2022
Listing Expires
December 31, 2027
Application
ANDA091567

Active Ingredients

IngredientStrength
Fexofenadine Hydrochloride180 mg/1

Drug Class

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

Selected Package

51660-0998-30Selected

1 BOTTLE in 1 CARTON (51660-998-30) / 30 TABLET, FILM COATED in 1 BOTTLE

Other packages for this product(1)

1 BOTTLE in 1 CARTON (51660-998-55) / 150 TABLET, FILM COATED in 1 BOTTLE