Visitor Monitoring Drug Details: ISOSORBIDE MONONITRATE
 
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Drug Details

Drug Name: ISOSORBIDE MONONITRATE
FDA Application No: (ANDA) 075448
Active Ingredient(s): ISOSORBIDE MONONITRATE
Company: IVAX PHARMS
Original Approval or Tentative Approval Date: June 19, 2000
 
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
ISOSORBIDE MONONITRATE ISOSORBIDE MONONITRATE60MGTABLET, EXTENDED RELEASE; ORAL Discontinued No None
ISOSORBIDE MONONITRATE ISOSORBIDE MONONITRATE30MGTABLET, EXTENDED RELEASE; ORAL Discontinued No None
ISOSORBIDE MONONITRATE ISOSORBIDE MONONITRATE120MGTABLET, EXTENDED RELEASE; ORAL Discontinued No None


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