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Benicar Hct - 54868-5075-1 - (olmesartan medoxomil and hydrochlorothiazide)

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Drug Information of Benicar Hct

Product NDC: 54868-5075
Proprietary Name: Benicar Hct
Non Proprietary Name: olmesartan medoxomil and hydrochlorothiazide
Active Ingredient(s): 12.5; 40    mg/1; mg/1 & nbsp;   olmesartan medoxomil and hydrochlorothiazide
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Benicar Hct

Product NDC: 54868-5075
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021532
Marketing Category: NDA
Start Marketing Date: 20040601

Package Information of Benicar Hct

Package NDC: 54868-5075-1
Package Description: 90 TABLET, FILM COATED in 1 BOTTLE (54868-5075-1)

NDC Information of Benicar Hct

NDC Code 54868-5075-1
Proprietary Name Benicar Hct
Package Description 90 TABLET, FILM COATED in 1 BOTTLE (54868-5075-1)
Product NDC 54868-5075
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name olmesartan medoxomil and hydrochlorothiazide
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20040601
Marketing Category Name NDA
Labeler Name Physicians Total Care, 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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