Visitor Monitoring Drug Details: ACEON
 
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Drug Details

Drug Name: ACEON
FDA Application No: (NDA) 020184
Active Ingredient(s): PERINDOPRIL ERBUMINE
Company: SOLVAY PHARMS
Original Approval or Tentative Approval Date: December 30, 1993
Chemical Type: 1 New molecular entity (NME)
Review Classification: S Standard review drug
 
There are no Therapeutic Equivalents Label Information
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
ACEON PERINDOPRIL ERBUMINE2MGTABLET; ORAL Prescription No None
ACEON PERINDOPRIL ERBUMINE4MGTABLET; ORAL Prescription No None
ACEON PERINDOPRIL ERBUMINE8MGTABLET; ORAL Prescription Yes None


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