Azor - 65597-111-90 - (amlodipine besylate and olmesartan medoxomil)

Alphabetical Index


Drug Information of Azor

Product NDC: 65597-111
Proprietary Name: Azor
Non Proprietary Name: amlodipine besylate and olmesartan medoxomil
Active Ingredient(s): 10; 20    mg/1; mg/1 & nbsp;   amlodipine besylate and olmesartan medoxomil
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Azor

Product NDC: 65597-111
Labeler Name: Daiichi Sankyo, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022100
Marketing Category: NDA
Start Marketing Date: 20070926

Package Information of Azor

Package NDC: 65597-111-90
Package Description: 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (65597-111-90)

NDC Information of Azor

NDC Code 65597-111-90
Proprietary Name Azor
Package Description 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (65597-111-90)
Product NDC 65597-111
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name amlodipine besylate and olmesartan medoxomil
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20070926
Marketing Category Name NDA
Labeler Name Daiichi Sankyo, Inc.
Substance Name AMLODIPINE BESYLATE; OLMESARTAN MEDOXOMIL
Strength Number 10; 20
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 Azor


General Information