Visitor Monitoring Drug Details: OMNITROPE
 
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Drug Details

Drug Name: OMNITROPE
FDA Application No: (NDA) 021426
Active Ingredient(s): SOMATROPIN RECOMBINANT
Company: SANDOZ
Original Approval or Tentative Approval Date: May 30, 2006
Chemical Type: 5 New manufacturer
Review Classification: S Standard 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
OMNITROPE SOMATROPIN RECOMBINANT5.8MG/VIALINJECTABLE; INJECTION Prescription No BX
OMNITROPE SOMATROPIN RECOMBINANT1.5MG/VIALINJECTABLE; INJECTION Prescription No BX


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