Visitor Monitoring Drug Details: REPRONEX
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
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Drug Details

Drug Name: REPRONEX
FDA Application No: (NDA) 021047
Active Ingredient(s): MENOTROPINS (FSH;LH)
Company: FERRING
Original Approval or Tentative Approval Date: August 27, 1999
Review Classification: S Standard review drug
 
There are no 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
REPRONEX MENOTROPINS (FSH;LH)75 IU/VIAL; 75 IU/VIALINJECTABLE; IM-SC Prescription Yes None
REPRONEX MENOTROPINS (FSH;LH)150 IU/VIAL; 150 IU/VIALINJECTABLE; INJECTION Discontinued No None


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