Xyzal - 0024-5800-90 - (levocetirizine dihydrochloride)

Alphabetical Index


Drug Information of Xyzal

Product NDC: 0024-5800
Proprietary Name: Xyzal
Non Proprietary Name: levocetirizine dihydrochloride
Active Ingredient(s): 5    mg/1 & nbsp;   levocetirizine dihydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Xyzal

Product NDC: 0024-5800
Labeler Name: Sanofi-Aventis U.S. LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022064
Marketing Category: NDA
Start Marketing Date: 20070809

Package Information of Xyzal

Package NDC: 0024-5800-90
Package Description: 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0024-5800-90)

NDC Information of Xyzal

NDC Code 0024-5800-90
Proprietary Name Xyzal
Package Description 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0024-5800-90)
Product NDC 0024-5800
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name levocetirizine dihydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20070809
Marketing Category Name NDA
Labeler Name Sanofi-Aventis U.S. LLC
Substance Name LEVOCETIRIZINE DIHYDROCHLORIDE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC]

Complete Information of Xyzal


General Information