Zyrtec - 50580-726-66 - (Cetirizine Hydrochloride)

Alphabetical Index


Drug Information of Zyrtec

Product NDC: 50580-726
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: 50580-726
Labeler Name: McNeil Consumer Healthcare Division of McNeil-PPC, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: NDA019835
Marketing Category: NDA
Start Marketing Date: 20081001

Package Information of Zyrtec

Package NDC: 50580-726-66
Package Description: 75 TABLET, FILM COATED in 1 PACKAGE, COMBINATION (50580-726-66)

NDC Information of Zyrtec

NDC Code 50580-726-66
Proprietary Name Zyrtec
Package Description 75 TABLET, FILM COATED in 1 PACKAGE, COMBINATION (50580-726-66)
Product NDC 50580-726
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Cetirizine Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20081001
Marketing Category Name NDA
Labeler Name McNeil Consumer Healthcare Division of McNeil-PPC, Inc.
Substance Name CETIRIZINE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Zyrtec


General Information