Visitor Monitoring Drug Details: NUTROPIN
 
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Drug Details

Drug Name: NUTROPIN
FDA Application No: (NDA) 020168
Active Ingredient(s): SOMATROPIN RECOMBINANT
Company: GENENTECH
Original Approval or Tentative Approval Date: November 17, 1993
Chemical Type: 5 New manufacturer
Review Classification: S Standard review drug
O Orphan drug
 
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
NUTROPIN SOMATROPIN RECOMBINANT5MG/VIALINJECTABLE; INJECTION Prescription No BX
NUTROPIN SOMATROPIN RECOMBINANT10MG/VIALINJECTABLE; INJECTION Prescription Yes None


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