Home > National Drug Code (NDC) > Levocetirizine Dihydrochloride

Levocetirizine Dihydrochloride - 63629-4492-1 - (Levocetirizine Dihydrochloride)

Alphabetical Index


Drug Information of Levocetirizine Dihydrochloride

Product NDC: 63629-4492
Proprietary Name: Levocetirizine Dihydrochloride
Non Proprietary Name: Levocetirizine Dihydrochloride
Active Ingredient(s): 5    mg/1 & nbsp;   Levocetirizine Dihydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Levocetirizine Dihydrochloride

Product NDC: 63629-4492
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090385
Marketing Category: ANDA
Start Marketing Date: 20110225

Package Information of Levocetirizine Dihydrochloride

Package NDC: 63629-4492-1
Package Description: 30 TABLET in 1 BOTTLE (63629-4492-1)

NDC Information of Levocetirizine Dihydrochloride

NDC Code 63629-4492-1
Proprietary Name Levocetirizine Dihydrochloride
Package Description 30 TABLET in 1 BOTTLE (63629-4492-1)
Product NDC 63629-4492
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Levocetirizine Dihydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110225
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
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 Levocetirizine Dihydrochloride


General Information