Visitor Monitoring Drug Details: PARAPLATIN
 
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Drug Details

Drug Name: PARAPLATIN
FDA Application No: (NDA) 019880
Active Ingredient(s): CARBOPLATIN
Company: BRISTOL MYERS SQUIBB
Original Approval or Tentative Approval Date: March 3, 1989
Chemical Type: 1 New molecular entity (NME)
Review Classification: P Priority review drug
 
Therapeutic Equivalents Label Information
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
PARAPLATIN CARBOPLATIN50MG/VIALINJECTABLE; INJECTION Discontinued No None
PARAPLATIN CARBOPLATIN150MG/VIALINJECTABLE; INJECTION Discontinued No None
PARAPLATIN CARBOPLATIN450MG/VIALINJECTABLE; INJECTION Discontinued No None


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