Exforge - 0078-0488-15 - (amlodipine besylate and valsartan)

Alphabetical Index


Drug Information of Exforge

Product NDC: 0078-0488
Proprietary Name: Exforge
Non Proprietary Name: amlodipine besylate and valsartan
Active Ingredient(s): 5; 160    mg/1; mg/1 & nbsp;   amlodipine besylate and valsartan
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Exforge

Product NDC: 0078-0488
Labeler Name: Novartis Pharmaceuticals Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021990
Marketing Category: NDA
Start Marketing Date: 20070620

Package Information of Exforge

Package NDC: 0078-0488-15
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (0078-0488-15)

NDC Information of Exforge

NDC Code 0078-0488-15
Proprietary Name Exforge
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (0078-0488-15)
Product NDC 0078-0488
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name amlodipine besylate and valsartan
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20070620
Marketing Category Name NDA
Labeler Name Novartis Pharmaceuticals Corporation
Substance Name AMLODIPINE BESYLATE; VALSARTAN
Strength Number 5; 160
Strength Unit mg/1; mg/1
Pharmaceutical Classes Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient],Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC]

Complete Information of Exforge


General Information