NDCFind

Fexofenadine Hydrochloride 68001-0439-00

Package NDC

68001-0439-00

Product NDC: 68001-0439

Manufacturer
Bluepoint Laboratories
Dosage Form
Tablet
Route
Oral
Product Type
Human Otc Drug
Marketing Start
June 19, 2020
Listing Expires
December 31, 2026
Application
ANDA076502

Active Ingredients

IngredientStrength
Fexofenadine Hydrochloride60 mg/1

Drug Class

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

Selected Package

68001-0439-00Selected

1 BOTTLE in 1 CARTON (68001-439-00) / 100 TABLET in 1 BOTTLE