Visitor Monitoring Drug Details: NADOLOL
 
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Drug Details

Drug Name: NADOLOL
FDA Application No: (ANDA) 074501
Active Ingredient(s): NADOLOL
Company: SANDOZ
Original Approval or Tentative Approval Date: November 9, 1995
 
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 NADOLOL20MGTABLET; ORAL Prescription No AB
NADOLOL NADOLOL40MGTABLET; ORAL Prescription No AB
NADOLOL NADOLOL80MGTABLET; ORAL Prescription No AB


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