Visitor Monitoring Drug Details: CAPOZIDE 25/15
 
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Drug Details

Drug Name: CAPOZIDE 25/15
FDA Application No: (NDA) 018709
Active Ingredient(s): CAPTOPRIL; HYDROCHLOROTHIAZIDE
Company: APOTHECON
Original Approval or Tentative Approval Date: October 12, 1984
Chemical Type: 4 New combination
Review Classification: S Standard review drug
 
There are no Therapeutic Equivalents Labels are not available
Approval History, Letters, Reviews and Related Documents
 
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Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
CAPOZIDE 25/15 CAPTOPRIL; HYDROCHLOROTHIAZIDE25MG; 15MGTABLET; ORAL Prescription No AB
CAPOZIDE 25/25 CAPTOPRIL; HYDROCHLOROTHIAZIDE25MG; 25MGTABLET; ORAL Prescription Yes AB
CAPOZIDE 50/15 CAPTOPRIL; HYDROCHLOROTHIAZIDE50MG; 15MGTABLET; ORAL Prescription Yes AB
CAPOZIDE 50/25 CAPTOPRIL; HYDROCHLOROTHIAZIDE50MG; 25MGTABLET; ORAL Prescription No AB


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