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Childrens Cetirizine Hydrochloride Hives Relief - 65862-443-48 - (Cetirizine Hydrochloride)

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Drug Information of Childrens Cetirizine Hydrochloride Hives Relief

Product NDC: 65862-443
Proprietary Name: Childrens Cetirizine Hydrochloride Hives Relief
Non Proprietary Name: Cetirizine Hydrochloride
Active Ingredient(s): 1    mg/mL & nbsp;   Cetirizine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Childrens Cetirizine Hydrochloride Hives Relief

Product NDC: 65862-443
Labeler Name: Aurobindo Pharma Limited
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA090750
Marketing Category: ANDA
Start Marketing Date: 20100202

Package Information of Childrens Cetirizine Hydrochloride Hives Relief

Package NDC: 65862-443-48
Package Description: 480 mL in 1 BOTTLE (65862-443-48)

NDC Information of Childrens Cetirizine Hydrochloride Hives Relief

NDC Code 65862-443-48
Proprietary Name Childrens Cetirizine Hydrochloride Hives Relief
Package Description 480 mL in 1 BOTTLE (65862-443-48)
Product NDC 65862-443
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Cetirizine Hydrochloride
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 20100202
Marketing Category Name ANDA
Labeler Name Aurobindo Pharma Limited
Substance Name CETIRIZINE HYDROCHLORIDE
Strength Number 1
Strength Unit mg/mL
Pharmaceutical Classes

Complete Information of Childrens Cetirizine Hydrochloride Hives Relief


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