Cetirizine - 63629-3708-7 - (Cetirizine Hydrochloride)

Alphabetical Index


Drug Information of Cetirizine

Product NDC: 63629-3708
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: 63629-3708
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA078336
Marketing Category: ANDA
Start Marketing Date: 20080116

Package Information of Cetirizine

Package NDC: 63629-3708-7
Package Description: 20 TABLET in 1 BOTTLE (63629-3708-7)

NDC Information of Cetirizine

NDC Code 63629-3708-7
Proprietary Name Cetirizine
Package Description 20 TABLET in 1 BOTTLE (63629-3708-7)
Product NDC 63629-3708
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Cetirizine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20080116
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
Substance Name CETIRIZINE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Cetirizine


General Information