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All Day Allergy Relief - 49348-984-46 - (Cetirizine HCl)

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Drug Information of All Day Allergy Relief

Product NDC: 49348-984
Proprietary Name: All Day Allergy Relief
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 Relief

Product NDC: 49348-984
Labeler Name: McKesson (Sunmark)
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA078780
Marketing Category: ANDA
Start Marketing Date: 20130315

Package Information of All Day Allergy Relief

Package NDC: 49348-984-46
Package Description: 1 BLISTER PACK in 1 CARTON (49348-984-46) > 14 TABLET in 1 BLISTER PACK

NDC Information of All Day Allergy Relief

NDC Code 49348-984-46
Proprietary Name All Day Allergy Relief
Package Description 1 BLISTER PACK in 1 CARTON (49348-984-46) > 14 TABLET in 1 BLISTER PACK
Product NDC 49348-984
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Cetirizine HCl
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130315
Marketing Category Name ANDA
Labeler Name McKesson (Sunmark)
Substance Name CETIRIZINE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of All Day Allergy Relief


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