Visitor Monitoring Drug Details: NADOLOL AND BENDROFLUMETHIAZIDE
 
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Drug Details

Drug Name: NADOLOL AND BENDROFLUMETHIAZIDE
FDA Application No: (ANDA) 077833
Active Ingredient(s): BENDROFLUMETHIAZIDE; NADOLOL
Company: IMPAX LABS
Original Approval or Tentative Approval Date: March 30, 2007
 
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
NADOLOL AND BENDROFLUMETHIAZIDE BENDROFLUMETHIAZIDE; NADOLOL5MG; 40MGTABLET; ORAL Prescription No AB
NADOLOL AND BENDROFLUMETHIAZIDE BENDROFLUMETHIAZIDE; NADOLOL5MG; 80MGTABLET; ORAL Prescription No AB


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