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Cetirizine Hydrochloride - 0093-6300-12 - (Cetirizine Hydrochloride)

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Drug Information of Cetirizine Hydrochloride

Product NDC: 0093-6300
Proprietary Name: Cetirizine Hydrochloride
Non Proprietary Name: Cetirizine Hydrochloride
Active Ingredient(s): 1    mg/mL & nbsp;   Cetirizine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): SYRUP
Coding System: National Drug Codes(NDC)

Labeler Information of Cetirizine Hydrochloride

Product NDC: 0093-6300
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077279
Marketing Category: ANDA
Start Marketing Date: 20080530

Package Information of Cetirizine Hydrochloride

Package NDC: 0093-6300-12
Package Description: 120 mL in 1 BOTTLE (0093-6300-12)

NDC Information of Cetirizine Hydrochloride

NDC Code 0093-6300-12
Proprietary Name Cetirizine Hydrochloride
Package Description 120 mL in 1 BOTTLE (0093-6300-12)
Product NDC 0093-6300
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cetirizine Hydrochloride
Dosage Form Name SYRUP
Route Name ORAL
Start Marketing Date 20080530
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA Inc
Substance Name CETIRIZINE HYDROCHLORIDE
Strength Number 1
Strength Unit mg/mL
Pharmaceutical Classes Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC]

Complete Information of Cetirizine Hydrochloride


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