Visitor Monitoring Drug Details: NEOSAR
 
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Drug Details

Drug Name: NEOSAR
FDA Application No: (NDA) 040015
Active Ingredient(s): CYCLOPHOSPHAMIDE
Company: TEVA PARENTERAL
Original Approval or Tentative Approval Date: April 29, 1993
 
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
NEOSAR CYCLOPHOSPHAMIDE100MG/VIALINJECTABLE; INJECTION Discontinued No None
NEOSAR CYCLOPHOSPHAMIDE200MG/VIALINJECTABLE; INJECTION Discontinued No None
NEOSAR CYCLOPHOSPHAMIDE500MG/VIALINJECTABLE; INJECTION Discontinued No None
NEOSAR CYCLOPHOSPHAMIDE1GM/VIALINJECTABLE; INJECTION Discontinued No None
NEOSAR CYCLOPHOSPHAMIDE2GM/VIALINJECTABLE; INJECTION Discontinued No None


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