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Cetirizine Hydrochloride - 65162-684-86 - (Cetirizine)

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Drug Information of Cetirizine Hydrochloride

Product NDC: 65162-684
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: 65162-684
Labeler Name: Amneal Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090766
Marketing Category: ANDA
Start Marketing Date: 20091007

Package Information of Cetirizine Hydrochloride

Package NDC: 65162-684-86
Package Description: 118 mL in 1 BOTTLE (65162-684-86)

NDC Information of Cetirizine Hydrochloride

NDC Code 65162-684-86
Proprietary Name Cetirizine Hydrochloride
Package Description 118 mL in 1 BOTTLE (65162-684-86)
Product NDC 65162-684
Product Type Name HUMAN PRESCRIPTION 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 Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC]

Complete Information of Cetirizine Hydrochloride


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