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Childrens Cetirizine Hydrochloride - 68016-023-43 - (Cetirizine Hydrochloride)

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Drug Information of Childrens Cetirizine Hydrochloride

Product NDC: 68016-023
Proprietary Name: Childrens Cetirizine Hydrochloride
Non Proprietary Name: Cetirizine Hydrochloride
Active Ingredient(s): 5    mg/5mL & nbsp;   Cetirizine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Childrens Cetirizine Hydrochloride

Product NDC: 68016-023
Labeler Name: Chain Drug Consortium, LLC (Premier Value)
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA090182
Marketing Category: ANDA
Start Marketing Date: 20080422

Package Information of Childrens Cetirizine Hydrochloride

Package NDC: 68016-023-43
Package Description: 1 BOTTLE in 1 CARTON (68016-023-43) > 120 mL in 1 BOTTLE

NDC Information of Childrens Cetirizine Hydrochloride

NDC Code 68016-023-43
Proprietary Name Childrens Cetirizine Hydrochloride
Package Description 1 BOTTLE in 1 CARTON (68016-023-43) > 120 mL in 1 BOTTLE
Product NDC 68016-023
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Cetirizine Hydrochloride
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 20080422
Marketing Category Name ANDA
Labeler Name Chain Drug Consortium, LLC (Premier Value)
Substance Name CETIRIZINE HYDROCHLORIDE
Strength Number 5
Strength Unit mg/5mL
Pharmaceutical Classes

Complete Information of Childrens Cetirizine Hydrochloride


General Information