Visitor Monitoring Drug Details: CARBOPLATIN
 
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Drug Details

Drug Name: CARBOPLATIN
FDA Application No: (ANDA) 077247
Active Ingredient(s): CARBOPLATIN
Company: ABRAXIS PHARM
Original Approval or Tentative Approval Date: October 21, 2004
 
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
CARBOPLATIN CARBOPLATINEQ 50MG/5ML (10MG/ML)INJECTABLE; IV (INFUSION) Discontinued No None
CARBOPLATIN CARBOPLATINEQ 150MG/15ML (10MG/ML)INJECTABLE; IV (INFUSION) Discontinued No None
CARBOPLATIN CARBOPLATINEQ 450MG/45ML (10MG/ML)INJECTABLE; IV (INFUSION) Prescription No AP


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