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Up and Up All Day Allergy Relief - 11673-458-66 - (Cetirizine Hydrochloride)

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Drug Information of Up and Up All Day Allergy Relief

Product NDC: 11673-458
Proprietary Name: Up and Up All Day Allergy Relief
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 Up and Up All Day Allergy Relief

Product NDC: 11673-458
Labeler Name: Target Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA078336
Marketing Category: ANDA
Start Marketing Date: 20090527

Package Information of Up and Up All Day Allergy Relief

Package NDC: 11673-458-66
Package Description: 1 BLISTER PACK in 1 CARTON (11673-458-66) > 14 TABLET in 1 BLISTER PACK

NDC Information of Up and Up All Day Allergy Relief

NDC Code 11673-458-66
Proprietary Name Up and Up All Day Allergy Relief
Package Description 1 BLISTER PACK in 1 CARTON (11673-458-66) > 14 TABLET in 1 BLISTER PACK
Product NDC 11673-458
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Cetirizine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090527
Marketing Category Name ANDA
Labeler Name Target Corporation
Substance Name CETIRIZINE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Up and Up All Day Allergy Relief


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