ZYRTEC - 50580-729-70 - (Cetirizine Hydrochloride)

Alphabetical Index


Drug Information of ZYRTEC

Product NDC: 50580-729
Proprietary Name: ZYRTEC
Non Proprietary Name: Cetirizine Hydrochloride
Active Ingredient(s): 10    mg/1 & nbsp;   Cetirizine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of ZYRTEC

Product NDC: 50580-729
Labeler Name: McNeil Consumer Healthcare Div McNeil-PPC, Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: NDA019835
Marketing Category: NDA
Start Marketing Date: 20080101

Package Information of ZYRTEC

Package NDC: 50580-729-70
Package Description: 1 BOTTLE, PLASTIC in 1 PACKAGE (50580-729-70) > 70 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

NDC Information of ZYRTEC

NDC Code 50580-729-70
Proprietary Name ZYRTEC
Package Description 1 BOTTLE, PLASTIC in 1 PACKAGE (50580-729-70) > 70 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Product NDC 50580-729
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Cetirizine Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20080101
Marketing Category Name NDA
Labeler Name McNeil Consumer Healthcare Div McNeil-PPC, Inc
Substance Name CETIRIZINE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of ZYRTEC


General Information