Visitor Monitoring Drug Details: NADOLOL
 
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Drug Details

Drug Name: NADOLOL
FDA Application No: (ANDA) 074255
Active Ingredient(s): NADOLOL
Company: IVAX PHARMS
Original Approval or Tentative Approval Date: January 24, 1996
 
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
NADOLOL NADOLOL80MGTABLET; ORAL Prescription No AB
NADOLOL NADOLOL120MGTABLET; ORAL Prescription No AB
NADOLOL NADOLOL160MGTABLET; ORAL Prescription No AB


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