Visitor Monitoring Drug Details: PENTOSTATIN
 
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Drug Details

Drug Name: PENTOSTATIN
FDA Application No: (ANDA) 077841
Active Ingredient(s): PENTOSTATIN
Company: BEDFORD LABS
Original Approval or Tentative Approval Date: August 7, 2007
 
 
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
PENTOSTATIN PENTOSTATIN10MG/VIALINJECTABLE; INJECTION Prescription No AP


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