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allergy relief - 11822-0458-3 - (Cetirizine Hydrochloride)

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Drug Information of allergy relief

Product NDC: 11822-0458
Proprietary Name: 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 allergy relief

Product NDC: 11822-0458
Labeler Name: Rite Aid Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA078336
Marketing Category: ANDA
Start Marketing Date: 20080116

Package Information of allergy relief

Package NDC: 11822-0458-3
Package Description: 1 BOTTLE in 1 CARTON (11822-0458-3) > 60 TABLET in 1 BOTTLE

NDC Information of allergy relief

NDC Code 11822-0458-3
Proprietary Name allergy relief
Package Description 1 BOTTLE in 1 CARTON (11822-0458-3) > 60 TABLET in 1 BOTTLE
Product NDC 11822-0458
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Cetirizine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20080116
Marketing Category Name ANDA
Labeler Name Rite Aid Corporation
Substance Name CETIRIZINE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of allergy relief


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