Visitor Monitoring Drug Details: SANDOSTATIN
 
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Drug Details

Drug Name: SANDOSTATIN
FDA Application No: (NDA) 019667
Active Ingredient(s): OCTREOTIDE ACETATE
Company: NOVARTIS
Original Approval or Tentative Approval Date: October 21, 1988
Chemical Type: 1 New molecular entity (NME)
Review Classification: P Priority review drug
 
 
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
SANDOSTATIN OCTREOTIDE ACETATEEQ 0.05MG BASE/MLINJECTABLE; INJECTION Prescription Yes AP
SANDOSTATIN OCTREOTIDE ACETATEEQ 0.1MG BASE/MLINJECTABLE; INJECTION Prescription Yes AP
SANDOSTATIN OCTREOTIDE ACETATEEQ 0.5MG BASE/MLINJECTABLE; INJECTION Prescription Yes AP
SANDOSTATIN OCTREOTIDE ACETATEEQ 0.2MG BASE/MLINJECTABLE; INJECTION Prescription Yes AP
SANDOSTATIN OCTREOTIDE ACETATEEQ 1MG BASE/MLINJECTABLE; INJECTION Prescription Yes AP


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On Monday, October 1, 2012 jeanne wrote:
 
can Octreatide cause a false possitive urin drug test? please reply asap !!!!
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