Azor - 54868-6036-0 - (amlodipine besylate and olmesartan medoxomil)

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Drug Information of Azor

Product NDC: 54868-6036
Proprietary Name: Azor
Non Proprietary Name: amlodipine besylate and olmesartan medoxomil
Active Ingredient(s): 5; 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: 54868-6036
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022100
Marketing Category: NDA
Start Marketing Date: 20090602

Package Information of Azor

Package NDC: 54868-6036-0
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54868-6036-0)

NDC Information of Azor

NDC Code 54868-6036-0
Proprietary Name Azor
Package Description 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54868-6036-0)
Product NDC 54868-6036
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 20090602
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name AMLODIPINE BESYLATE; OLMESARTAN MEDOXOMIL
Strength Number 5; 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