Visitor Monitoring Drug Details: BENICAR HCT
 
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Drug Details

Drug Name: BENICAR HCT
FDA Application No: (NDA) 021532
Active Ingredient(s): HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL
Company: DAIICHI SANKYO
Original Approval or Tentative Approval Date: June 5, 2003
Chemical Type: 4 New combination
Review Classification: S Standard review drug
 
There are no Therapeutic Equivalents Label Information
Approval History, Letters, Reviews and Related Documents
 
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Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
BENICAR HCT HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL12.5MG; 20MGTABLET; ORAL Prescription No None
BENICAR HCT HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL12.5MG; 40MGTABLET; ORAL Prescription No None
BENICAR HCT HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL25MG; 40MGTABLET; ORAL Prescription Yes None


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