Amturnide - 0078-0613-15 - (Aliskiren Hemifumarate and Amlodipine Besylate and Hydrochlorothiazide)

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Drug Information of Amturnide

Product NDC: 0078-0613
Proprietary Name: Amturnide
Non Proprietary Name: Aliskiren Hemifumarate and Amlodipine Besylate and Hydrochlorothiazide
Active Ingredient(s): 300; 10; 12.5    mg/1; mg/1; mg/1 & nbsp;   Aliskiren Hemifumarate and Amlodipine Besylate and Hydrochlorothiazide
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Amturnide

Product NDC: 0078-0613
Labeler Name: Novartis Pharmaceuticals Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA200045
Marketing Category: NDA
Start Marketing Date: 20101221

Package Information of Amturnide

Package NDC: 0078-0613-15
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (0078-0613-15)

NDC Information of Amturnide

NDC Code 0078-0613-15
Proprietary Name Amturnide
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (0078-0613-15)
Product NDC 0078-0613
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Aliskiren Hemifumarate and Amlodipine Besylate and Hydrochlorothiazide
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20101221
Marketing Category Name NDA
Labeler Name Novartis Pharmaceuticals Corporation
Substance Name ALISKIREN HEMIFUMARATE; AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE
Strength Number 300; 10; 12.5
Strength Unit mg/1; mg/1; mg/1
Pharmaceutical Classes Renin Inhibitor [EPC],Renin Inhibitors [MoA],Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient]

Complete Information of Amturnide


General Information