Visitor Monitoring Drug Details: INDERIDE LA 160/50
 
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Drug Details

Drug Name: INDERIDE LA 160/50
FDA Application No: (NDA) 019059
Active Ingredient(s): HYDROCHLOROTHIAZIDE; PROPRANOLOL HYDROCHLORIDE
Company: WYETH AYERST
Original Approval or Tentative Approval Date: July 3, 1985
Chemical Type: 3 New dosage form
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
INDERIDE LA 120/50 HYDROCHLOROTHIAZIDE; PROPRANOLOL HYDROCHLORIDE50MG; 120MGCAPSULE, EXTENDED RELEASE; ORAL Discontinued No None
INDERIDE LA 160/50 HYDROCHLOROTHIAZIDE; PROPRANOLOL HYDROCHLORIDE50MG; 160MGCAPSULE, EXTENDED RELEASE; ORAL Discontinued No None
INDERIDE LA 80/50 HYDROCHLOROTHIAZIDE; PROPRANOLOL HYDROCHLORIDE50MG; 80MGCAPSULE, EXTENDED RELEASE; ORAL Discontinued No None


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