Visitor Monitoring Drug Details: HUMATROPE
 
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Drug Details

Drug Name: HUMATROPE
FDA Application No: (NDA) 019640
Active Ingredient(s): SOMATROPIN RECOMBINANT
Company: LILLY
Original Approval or Tentative Approval Date: March 8, 1987
Chemical Type: 5 New manufacturer
Review Classification: P Priority review drug
O Orphan drug
 
Therapeutic Equivalents Label Information
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
HUMATROPE SOMATROPIN RECOMBINANT2MG/VIALINJECTABLE; INJECTION Discontinued No None
HUMATROPE SOMATROPIN RECOMBINANT5MG/VIALINJECTABLE; INJECTION Prescription Yes BX
HUMATROPE SOMATROPIN RECOMBINANT6MG/VIALINJECTABLE; INJECTION Prescription No BX
HUMATROPE SOMATROPIN RECOMBINANT12MG/VIALINJECTABLE; INJECTION Prescription Yes None
HUMATROPE SOMATROPIN RECOMBINANT24MG/VIALINJECTABLE; INJECTION Prescription Yes None


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