Visitor Monitoring Drug Details: TENORMIN
 
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Drug Details

Drug Name: TENORMIN
FDA Application No: (NDA) 018240
Active Ingredient(s): ATENOLOL
Company: ASTRAZENECA
Original Approval or Tentative Approval Date: August 19, 1981
Chemical Type: 1 New molecular entity (NME)
Review Classification: S Standard review drug
 
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
TENORMIN ATENOLOL50MGTABLET; ORAL Prescription No AB
TENORMIN ATENOLOL100MGTABLET; ORAL Prescription Yes AB
TENORMIN ATENOLOL25MGTABLET; ORAL Prescription No AB


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