ZYRTEC-D - 50580-728-52 - (Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride)

Alphabetical Index


Drug Information of ZYRTEC-D

Product NDC: 50580-728
Proprietary Name: ZYRTEC-D
Non Proprietary Name: Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride
Active Ingredient(s): 5; 120    mg/1; mg/1 & nbsp;   Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of ZYRTEC-D

Product NDC: 50580-728
Labeler Name: McNeil Consumer Healthcare Div McNeil-PPC, Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: NDA021150
Marketing Category: NDA
Start Marketing Date: 20080101

Package Information of ZYRTEC-D

Package NDC: 50580-728-52
Package Description: 24 BLISTER PACK in 1 CARTON (50580-728-52) > 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

NDC Information of ZYRTEC-D

NDC Code 50580-728-52
Proprietary Name ZYRTEC-D
Package Description 24 BLISTER PACK in 1 CARTON (50580-728-52) > 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Product NDC 50580-728
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20080101
Marketing Category Name NDA
Labeler Name McNeil Consumer Healthcare Div McNeil-PPC, Inc
Substance Name CETIRIZINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE
Strength Number 5; 120
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of ZYRTEC-D


General Information