NDCFind

Cetirizine Hydrochloride 51672-4070-08

Package NDC

51672-4070-08

Product NDC: 51672-4070

Manufacturer
Sun Pharmaceutical Industries, Inc.
Dosage Form
Solution
Route
Oral
Product Type
Human Prescription Drug
Marketing Start
May 1, 2014
Listing Expires
December 31, 2026
Application
ANDA076601
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Active Ingredients

IngredientStrength
Cetirizine Hydrochloride1 mg/mL

Drug Class

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

Selected Package

51672-4070-08Selected

1 BOTTLE in 1 CARTON (51672-4070-8) / 120 mL in 1 BOTTLE