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Berkley and Jensen Cetirizine Hydrochloride - 68391-458-88 - (Cetirizine Hydrochloride)

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Drug Information of Berkley and Jensen Cetirizine Hydrochloride

Product NDC: 68391-458
Proprietary Name: Berkley and Jensen 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 Berkley and Jensen Cetirizine Hydrochloride

Product NDC: 68391-458
Labeler Name: BJWC
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA078336
Marketing Category: ANDA
Start Marketing Date: 20090427

Package Information of Berkley and Jensen Cetirizine Hydrochloride

Package NDC: 68391-458-88
Package Description: 1 BOTTLE in 1 PACKAGE (68391-458-88) > 365 TABLET in 1 BOTTLE

NDC Information of Berkley and Jensen Cetirizine Hydrochloride

NDC Code 68391-458-88
Proprietary Name Berkley and Jensen Cetirizine Hydrochloride
Package Description 1 BOTTLE in 1 PACKAGE (68391-458-88) > 365 TABLET in 1 BOTTLE
Product NDC 68391-458
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Cetirizine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090427
Marketing Category Name ANDA
Labeler Name BJWC
Substance Name CETIRIZINE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Berkley and Jensen Cetirizine Hydrochloride


General Information