Visitor Monitoring Drug Details: UNIRETIC
 
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Drug Details

Drug Name: UNIRETIC
FDA Application No: (NDA) 020729
Active Ingredient(s): HYDROCHLOROTHIAZIDE; MOEXIPRIL HYDROCHLORIDE
Company: SCHWARZ PHARMA
Original Approval or Tentative Approval Date: June 27, 1997
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
UNIRETIC HYDROCHLOROTHIAZIDE; MOEXIPRIL HYDROCHLORIDE12.5MG; 7.5MGTABLET; ORAL Prescription No AB
UNIRETIC HYDROCHLOROTHIAZIDE; MOEXIPRIL HYDROCHLORIDE25MG; 15MGTABLET; ORAL Prescription Yes AB
UNIRETIC HYDROCHLOROTHIAZIDE; MOEXIPRIL HYDROCHLORIDE12.5MG; 15MGTABLET; ORAL Prescription No AB


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