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All Day Allergy - 59726-220-14 - (Cetirizine HCl)

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Drug Information of All Day Allergy

Product NDC: 59726-220
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: 59726-220
Labeler Name: P and L Development of New York Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA078427
Marketing Category: ANDA
Start Marketing Date: 20121205

Package Information of All Day Allergy

Package NDC: 59726-220-14
Package Description: 1 BLISTER PACK in 1 CARTON (59726-220-14) > 14 TABLET in 1 BLISTER PACK

NDC Information of All Day Allergy

NDC Code 59726-220-14
Proprietary Name All Day Allergy
Package Description 1 BLISTER PACK in 1 CARTON (59726-220-14) > 14 TABLET in 1 BLISTER PACK
Product NDC 59726-220
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Cetirizine HCl
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20121205
Marketing Category Name ANDA
Labeler Name P and L Development of New York Corporation
Substance Name CETIRIZINE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of All Day Allergy


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