Visitor Monitoring Drug Details: CARBOPLATIN
 
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Drug Details

Drug Name: CARBOPLATIN
FDA Application No: (ANDA) 077269
Active Ingredient(s): CARBOPLATIN
Company: PHARMACHEMIE
Original Approval or Tentative Approval Date: October 14, 2004
 
 
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 CARBOPLATINEQ 50MG/5ML (10MG/ML)INJECTABLE; IV (INFUSION) Prescription Yes AP
CARBOPLATIN CARBOPLATINEQ 150MG/15ML (10MG/ML)INJECTABLE; IV (INFUSION) Prescription Yes AP
CARBOPLATIN CARBOPLATINEQ 450MG/45ML (10MG/ML)INJECTABLE; IV (INFUSION) Prescription Yes AP


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