NDCFind

Childrens Fexofenadine Hydrochloride Allergy 51672-2141-01

Generic: Fexofenadine Hydrochloride

Package NDC

51672-2141-01

Product NDC: 51672-2141

Manufacturer
Sun Pharmaceutical Industries, Inc.
Dosage Form
Suspension
Route
Oral
Product Type
Human Otc Drug
Marketing Start
January 24, 2024
Listing Expires
December 31, 2027
Application
ANDA208123

Active Ingredients

IngredientStrength
Fexofenadine Hydrochloride30 mg/5mL

Drug Class

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

Selected Package

51672-2141-01Selected

1 BOTTLE in 1 CARTON (51672-2141-1) / 240 mL in 1 BOTTLE

Other packages for this product(1)

1 BOTTLE in 1 CARTON (51672-2141-8) / 120 mL in 1 BOTTLE