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Cetirizine Hydrochloride - 52125-332-20 - (Cetirizine Hydrochloride)

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Drug Information of Cetirizine Hydrochloride

Product NDC: 52125-332
Proprietary Name: Cetirizine Hydrochloride
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 Cetirizine Hydrochloride

Product NDC: 52125-332
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077829
Marketing Category: ANDA
Start Marketing Date: 20130603

Package Information of Cetirizine Hydrochloride

Package NDC: 52125-332-20
Package Description: 100 TABLET in 1 VIAL (52125-332-20)

NDC Information of Cetirizine Hydrochloride

NDC Code 52125-332-20
Proprietary Name Cetirizine Hydrochloride
Package Description 100 TABLET in 1 VIAL (52125-332-20)
Product NDC 52125-332
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cetirizine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130603
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name CETIRIZINE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC]

Complete Information of Cetirizine Hydrochloride


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