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Childrens Cetirizine Hydrochloride - 62011-0093-1 - (Cetirizine hydrochloride)

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Drug Information of Childrens Cetirizine Hydrochloride

Product NDC: 62011-0093
Proprietary Name: Childrens Cetirizine Hydrochloride
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

Product NDC: 62011-0093
Labeler Name: Health Mart
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA201546
Marketing Category: ANDA
Start Marketing Date: 20110520

Package Information of Childrens Cetirizine Hydrochloride

Package NDC: 62011-0093-1
Package Description: 1 BOTTLE in 1 CARTON (62011-0093-1) > 118 mL in 1 BOTTLE

NDC Information of Childrens Cetirizine Hydrochloride

NDC Code 62011-0093-1
Proprietary Name Childrens Cetirizine Hydrochloride
Package Description 1 BOTTLE in 1 CARTON (62011-0093-1) > 118 mL in 1 BOTTLE
Product NDC 62011-0093
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Cetirizine hydrochloride
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 20110520
Marketing Category Name ANDA
Labeler Name Health Mart
Substance Name CETIRIZINE HYDROCHLORIDE
Strength Number 1
Strength Unit mg/mL
Pharmaceutical Classes

Complete Information of Childrens Cetirizine Hydrochloride


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