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Cetirizine Hydrochloride - 47335-343-83 - (Cetirizine Hydrochloride)

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Drug Information of Cetirizine Hydrochloride

Product NDC: 47335-343
Proprietary Name: Cetirizine Hydrochloride
Non Proprietary Name: Cetirizine Hydrochloride
Active Ingredient(s): 5    mg/1 & nbsp;   Cetirizine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, CHEWABLE
Coding System: National Drug Codes(NDC)

Labeler Information of Cetirizine Hydrochloride

Product NDC: 47335-343
Labeler Name: Sun Pharma Global FZE
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA090142
Marketing Category: ANDA
Start Marketing Date: 20110909

Package Information of Cetirizine Hydrochloride

Package NDC: 47335-343-83
Package Description: 30 TABLET, CHEWABLE in 1 BOTTLE (47335-343-83)

NDC Information of Cetirizine Hydrochloride

NDC Code 47335-343-83
Proprietary Name Cetirizine Hydrochloride
Package Description 30 TABLET, CHEWABLE in 1 BOTTLE (47335-343-83)
Product NDC 47335-343
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Cetirizine Hydrochloride
Dosage Form Name TABLET, CHEWABLE
Route Name ORAL
Start Marketing Date 20110909
Marketing Category Name ANDA
Labeler Name Sun Pharma Global FZE
Substance Name CETIRIZINE HYDROCHLORIDE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Cetirizine Hydrochloride


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