Cetirizine - 0615-7522-39 - (Cetirizine Hydrochloride)

Alphabetical Index


Drug Information of Cetirizine

Product NDC: 0615-7522
Proprietary Name: Cetirizine
Non Proprietary Name: Cetirizine Hydrochloride
Active Ingredient(s): 10    mg/1 & nbsp;   Cetirizine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Cetirizine

Product NDC: 0615-7522
Labeler Name: NCS HealthCare of KY, Inc dba Vangard Labs
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA077946
Marketing Category: ANDA
Start Marketing Date: 20071227

Package Information of Cetirizine

Package NDC: 0615-7522-39
Package Description: 30 TABLET in 1 BLISTER PACK (0615-7522-39)

NDC Information of Cetirizine

NDC Code 0615-7522-39
Proprietary Name Cetirizine
Package Description 30 TABLET in 1 BLISTER PACK (0615-7522-39)
Product NDC 0615-7522
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Cetirizine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20071227
Marketing Category Name ANDA
Labeler Name NCS HealthCare of KY, Inc dba Vangard Labs
Substance Name CETIRIZINE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Cetirizine


General Information