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CHILDRENS ALLERGY - 37808-884-26 - (cetirizine Hydrochloride)

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Drug Information of CHILDRENS ALLERGY

Product NDC: 37808-884
Proprietary Name: CHILDRENS ALLERGY
Non Proprietary Name: cetirizine Hydrochloride
Active Ingredient(s): 5    mg/5mL & nbsp;   cetirizine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of CHILDRENS ALLERGY

Product NDC: 37808-884
Labeler Name: H E B
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA090254
Marketing Category: ANDA
Start Marketing Date: 20101101

Package Information of CHILDRENS ALLERGY

Package NDC: 37808-884-26
Package Description: 1 BOTTLE in 1 CARTON (37808-884-26) > 118 mL in 1 BOTTLE

NDC Information of CHILDRENS ALLERGY

NDC Code 37808-884-26
Proprietary Name CHILDRENS ALLERGY
Package Description 1 BOTTLE in 1 CARTON (37808-884-26) > 118 mL in 1 BOTTLE
Product NDC 37808-884
Product Type Name HUMAN OTC DRUG
Non Proprietary Name cetirizine Hydrochloride
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20101101
Marketing Category Name ANDA
Labeler Name H E B
Substance Name CETIRIZINE HYDROCHLORIDE
Strength Number 5
Strength Unit mg/5mL
Pharmaceutical Classes

Complete Information of CHILDRENS ALLERGY


General Information