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Cetirizine Hydrochloride - 0781-5283-64 - (Cetirizine Hydrochloride)

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Drug Information of Cetirizine Hydrochloride

Product NDC: 0781-5283
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, CHEWABLE
Coding System: National Drug Codes(NDC)

Labeler Information of Cetirizine Hydrochloride

Product NDC: 0781-5283
Labeler Name: Sandoz Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA078692
Marketing Category: ANDA
Start Marketing Date: 20080214

Package Information of Cetirizine Hydrochloride

Package NDC: 0781-5283-64
Package Description: 30 TABLET, CHEWABLE in 1 BOX, UNIT-DOSE (0781-5283-64)

NDC Information of Cetirizine Hydrochloride

NDC Code 0781-5283-64
Proprietary Name Cetirizine Hydrochloride
Package Description 30 TABLET, CHEWABLE in 1 BOX, UNIT-DOSE (0781-5283-64)
Product NDC 0781-5283
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Cetirizine Hydrochloride
Dosage Form Name TABLET, CHEWABLE
Route Name ORAL
Start Marketing Date 20080214
Marketing Category Name ANDA
Labeler Name Sandoz Inc
Substance Name CETIRIZINE HYDROCHLORIDE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Cetirizine Hydrochloride


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