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Cetirizine Hydrochloride - 65162-005-86 - (Cetirizine)

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Drug Information of Cetirizine Hydrochloride

Product NDC: 65162-005
Proprietary Name: Cetirizine Hydrochloride
Non Proprietary Name: Cetirizine
Active Ingredient(s): 5    mg/5mL & nbsp;   Cetirizine
Administration Route(s): ORAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Cetirizine Hydrochloride

Product NDC: 65162-005
Labeler Name: Amneal Pharmaceuticals
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA090765
Marketing Category: ANDA
Start Marketing Date: 20091007

Package Information of Cetirizine Hydrochloride

Package NDC: 65162-005-86
Package Description: 1 BOTTLE in 1 CARTON (65162-005-86) > 118 mL in 1 BOTTLE

NDC Information of Cetirizine Hydrochloride

NDC Code 65162-005-86
Proprietary Name Cetirizine Hydrochloride
Package Description 1 BOTTLE in 1 CARTON (65162-005-86) > 118 mL in 1 BOTTLE
Product NDC 65162-005
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Cetirizine
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 20091007
Marketing Category Name ANDA
Labeler Name Amneal Pharmaceuticals
Substance Name CETIRIZINE HYDROCHLORIDE
Strength Number 5
Strength Unit mg/5mL
Pharmaceutical Classes

Complete Information of Cetirizine Hydrochloride


General Information