Visitor Monitoring Drug Details: INDERIDE-80/25
 
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Drug Details

Drug Name: INDERIDE-80/25
FDA Application No: (NDA) 018031
Active Ingredient(s): HYDROCHLOROTHIAZIDE; PROPRANOLOL HYDROCHLORIDE
Company: WYETH PHARMS INC
Original Approval or Tentative Approval Date: June 15, 1979
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
 
You can see the products in the same application. The table can be sorted by clicking the header columns.
 
Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
INDERIDE-40/25 HYDROCHLOROTHIAZIDE; PROPRANOLOL HYDROCHLORIDE25MG; 40MGTABLET; ORAL Prescription Yes AB
INDERIDE-80/25 HYDROCHLOROTHIAZIDE; PROPRANOLOL HYDROCHLORIDE25MG; 80MGTABLET; ORAL Discontinued No None


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