Visitor Monitoring Drug Details: PEMOLINE
 
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Drug Details

Drug Name: PEMOLINE
FDA Application No: (ANDA) 075286
Active Ingredient(s): PEMOLINE
Company: SANDOZ
Original Approval or Tentative Approval Date: June 30, 1999
 
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
PEMOLINE PEMOLINE18.75MGTABLET; ORAL Discontinued No None
PEMOLINE PEMOLINE37.5MGTABLET; ORAL Discontinued No None
PEMOLINE PEMOLINE75MGTABLET; ORAL Discontinued No None


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