Visitor Monitoring Drug Details: RAPLON
 
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Drug Details

Drug Name: RAPLON
FDA Application No: (NDA) 020984
Active Ingredient(s): RAPACURONIUM BROMIDE
Company: ORGANON USA INC
Original Approval or Tentative Approval Date: August 18, 1999
Chemical Type: 1 New molecular entity (NME)
Review Classification: S Standard review drug
 
There are no 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
RAPLON RAPACURONIUM BROMIDE100MG/VIALINJECTABLE; INJECTION Discontinued No None
RAPLON RAPACURONIUM BROMIDE200MG/VIALINJECTABLE; INJECTION Discontinued No None


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