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Leader All Day Allergy - 37205-825-74 - (Cetirizine Hydrochloride)

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Drug Information of Leader All Day Allergy

Product NDC: 37205-825
Proprietary Name: Leader All Day Allergy
Non Proprietary Name: Cetirizine Hydrochloride
Active Ingredient(s): 10    mg/1 & nbsp;   Cetirizine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Leader All Day Allergy

Product NDC: 37205-825
Labeler Name: Cardinal Health
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA078336
Marketing Category: ANDA
Start Marketing Date: 20080116

Package Information of Leader All Day Allergy

Package NDC: 37205-825-74
Package Description: 1 BLISTER PACK in 1 CARTON (37205-825-74) > 14 TABLET in 1 BLISTER PACK

NDC Information of Leader All Day Allergy

NDC Code 37205-825-74
Proprietary Name Leader All Day Allergy
Package Description 1 BLISTER PACK in 1 CARTON (37205-825-74) > 14 TABLET in 1 BLISTER PACK
Product NDC 37205-825
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Cetirizine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20080116
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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