Visitor Monitoring Drug Details: ZIAC
 
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Drug Details

Drug Name: ZIAC
FDA Application No: (NDA) 020186
Active Ingredient(s): BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE
Company: DURAMED PHARMS BARR
Original Approval or Tentative Approval Date: March 26, 1993
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
ZIAC BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE5MG; 6.25MGTABLET; ORAL Prescription No AB
ZIAC BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE10MG; 6.25MGTABLET; ORAL Prescription Yes AB
ZIAC BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE2.5MG; 6.25MGTABLET; ORAL Prescription No AB


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