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CETIRIZINE HYDROCHLORIDE - 49349-088-02 - (CETIRIZINE HYDROCHLORIDE)

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Drug Information of CETIRIZINE HYDROCHLORIDE

Product NDC: 49349-088
Proprietary Name: CETIRIZINE HYDROCHLORIDE
Non Proprietary Name: CETIRIZINE HYDROCHLORIDE
Active Ingredient(s): 5    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: 49349-088
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078317
Marketing Category: ANDA
Start Marketing Date: 20101123

Package Information of CETIRIZINE HYDROCHLORIDE

Package NDC: 49349-088-02
Package Description: 30 TABLET in 1 BLISTER PACK (49349-088-02)

NDC Information of CETIRIZINE HYDROCHLORIDE

NDC Code 49349-088-02
Proprietary Name CETIRIZINE HYDROCHLORIDE
Package Description 30 TABLET in 1 BLISTER PACK (49349-088-02)
Product NDC 49349-088
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name CETIRIZINE HYDROCHLORIDE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20101123
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name CETIRIZINE HYDROCHLORIDE
Strength Number 5
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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