Visitor Monitoring Drug Details: LUPRON
 
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Drug Details

Drug Name: LUPRON
FDA Application No: (NDA) 019943
Active Ingredient(s): LEUPROLIDE ACETATE
Company: TAP PHARM
Original Approval or Tentative Approval Date: March 30, 1995
Chemical Type: 5 New manufacturer
Review Classification: S Standard review drug
 
There are no 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
LUPRON LEUPROLIDE ACETATE7.5MGSuspension; Depot Prescription No None
LUPRON LEUPROLIDE ACETATE3.75MGSuspension; Depot Prescription No None
LUPRON LEUPROLIDE ACETATE22.5MGSuspension; Depot Prescription No None
LUPRON LEUPROLIDE ACETATE11.25MGSuspension; Depot Prescription No None


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