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LEADER ALL DAY ALLERGY - 37205-820-75 - (cetirizine)

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Drug Information of LEADER ALL DAY ALLERGY

Product NDC: 37205-820
Proprietary Name: LEADER ALL DAY ALLERGY
Non Proprietary Name: cetirizine
Active Ingredient(s): 10    mg/1 & nbsp;   cetirizine
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of LEADER ALL DAY ALLERGY

Product NDC: 37205-820
Labeler Name: Cardinal Health
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA077498
Marketing Category: ANDA
Start Marketing Date: 20071227

Package Information of LEADER ALL DAY ALLERGY

Package NDC: 37205-820-75
Package Description: 90 TABLET in 1 BOTTLE (37205-820-75)

NDC Information of LEADER ALL DAY ALLERGY

NDC Code 37205-820-75
Proprietary Name LEADER ALL DAY ALLERGY
Package Description 90 TABLET in 1 BOTTLE (37205-820-75)
Product NDC 37205-820
Product Type Name HUMAN OTC DRUG
Non Proprietary Name cetirizine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20071227
Marketing Category Name ANDA
Labeler Name Cardinal Health
Substance Name CETIRIZINE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of LEADER ALL DAY ALLERGY


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