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Allergy Relief - 55910-129-45 - (Cetirizine HCl)

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Drug Information of Allergy Relief

Product NDC: 55910-129
Proprietary Name: 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 Allergy Relief

Product NDC: 55910-129
Labeler Name: Dolgencorp, Inc. (DOLLAR GENERAL & REXALL)
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA078780
Marketing Category: ANDA
Start Marketing Date: 20130517

Package Information of Allergy Relief

Package NDC: 55910-129-45
Package Description: 1 BOTTLE, PLASTIC in 1 BOX (55910-129-45) > 45 TABLET in 1 BOTTLE, PLASTIC

NDC Information of Allergy Relief

NDC Code 55910-129-45
Proprietary Name Allergy Relief
Package Description 1 BOTTLE, PLASTIC in 1 BOX (55910-129-45) > 45 TABLET in 1 BOTTLE, PLASTIC
Product NDC 55910-129
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Cetirizine HCl
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130517
Marketing Category Name ANDA
Labeler Name Dolgencorp, Inc. (DOLLAR GENERAL & REXALL)
Substance Name CETIRIZINE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Allergy Relief


General Information