Visitor Monitoring Drug Details: CARBOPLATIN
 
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Drug Details

Drug Name: CARBOPLATIN
FDA Application No: (ANDA) 076039
Active Ingredient(s): CARBOPLATIN
Company: BEDFORD LABS
Original Approval or Tentative Approval Date: June 6, 2003
 
 
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
CARBOPLATIN CARBOPLATIN10MG/MLInjectable; Injection Prescription No None


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