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Childrens Cetirizine Hydrochloride Allergy - 65862-422-12 - (Cetirizine Hydrochloride)

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Drug Information of Childrens Cetirizine Hydrochloride Allergy

Product NDC: 65862-422
Proprietary Name: Childrens Cetirizine Hydrochloride Allergy
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 Allergy

Product NDC: 65862-422
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 Allergy

Package NDC: 65862-422-12
Package Description: 1 BOTTLE in 1 CARTON (65862-422-12) > 120 mL in 1 BOTTLE

NDC Information of Childrens Cetirizine Hydrochloride Allergy

NDC Code 65862-422-12
Proprietary Name Childrens Cetirizine Hydrochloride Allergy
Package Description 1 BOTTLE in 1 CARTON (65862-422-12) > 120 mL in 1 BOTTLE
Product NDC 65862-422
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 Allergy


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