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leader childrens all day allergy - 37205-855-26 - (cetirizine Hydrochloride)

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Drug Information of leader childrens all day allergy

Product NDC: 37205-855
Proprietary Name: leader childrens all day 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 leader childrens all day allergy

Product NDC: 37205-855
Labeler Name: Cardinal Health
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA090254
Marketing Category: ANDA
Start Marketing Date: 20101109

Package Information of leader childrens all day allergy

Package NDC: 37205-855-26
Package Description: 1 BOTTLE in 1 CARTON (37205-855-26) > 120 mL in 1 BOTTLE

NDC Information of leader childrens all day allergy

NDC Code 37205-855-26
Proprietary Name leader childrens all day allergy
Package Description 1 BOTTLE in 1 CARTON (37205-855-26) > 120 mL in 1 BOTTLE
Product NDC 37205-855
Product Type Name HUMAN OTC DRUG
Non Proprietary Name cetirizine Hydrochloride
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20101109
Marketing Category Name ANDA
Labeler Name Cardinal Health
Substance Name CETIRIZINE HYDROCHLORIDE
Strength Number 5
Strength Unit mg/5mL
Pharmaceutical Classes

Complete Information of leader childrens all day allergy


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