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All Day Allergy - 62011-0205-2 - (Cetirizine HCl)

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Drug Information of All Day Allergy

Product NDC: 62011-0205
Proprietary Name: All Day Allergy
Non Proprietary Name: Cetirizine HCl
Active Ingredient(s): 10    mg/1 & nbsp;   Cetirizine HCl
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of All Day Allergy

Product NDC: 62011-0205
Labeler Name: McKesson (Health Mart)
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA078780
Marketing Category: ANDA
Start Marketing Date: 20120101

Package Information of All Day Allergy

Package NDC: 62011-0205-2
Package Description: 2 BLISTER PACK in 1 CARTON (62011-0205-2) > 15 TABLET in 1 BLISTER PACK

NDC Information of All Day Allergy

NDC Code 62011-0205-2
Proprietary Name All Day Allergy
Package Description 2 BLISTER PACK in 1 CARTON (62011-0205-2) > 15 TABLET in 1 BLISTER PACK
Product NDC 62011-0205
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Cetirizine HCl
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120101
Marketing Category Name ANDA
Labeler Name McKesson (Health Mart)
Substance Name CETIRIZINE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of All Day Allergy


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