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Benicar HCT - 65597-106-11 - (olmesartan medoxomil-hydrochlorothiazide)

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Drug Information of Benicar HCT

Product NDC: 65597-106
Proprietary Name: Benicar HCT
Non Proprietary Name: olmesartan medoxomil-hydrochlorothiazide
Active Ingredient(s): 12.5; 40    mg/1; mg/1 & nbsp;   olmesartan medoxomil-hydrochlorothiazide
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Benicar HCT

Product NDC: 65597-106
Labeler Name: Daiichi Sankyo, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021532
Marketing Category: NDA
Start Marketing Date: 20030605

Package Information of Benicar HCT

Package NDC: 65597-106-11
Package Description: 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (65597-106-11)

NDC Information of Benicar HCT

NDC Code 65597-106-11
Proprietary Name Benicar HCT
Package Description 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (65597-106-11)
Product NDC 65597-106
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name olmesartan medoxomil-hydrochlorothiazide
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20030605
Marketing Category Name NDA
Labeler Name Daiichi Sankyo, Inc.
Substance Name HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL
Strength Number 12.5; 40
Strength Unit mg/1; mg/1
Pharmaceutical Classes Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient]

Complete Information of Benicar HCT


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