Visitor Monitoring Drug History: REPRONEX
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
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Label and Approval History

Drug Name: REPRONEX
FDA Application No: (NDA) 021047
Active Ingredient(s): MENOTROPINS (FSH;LH)
Company: FERRING
 
Label History
 
View the label approved on August 27, 1999 for REPRONEX, (NDA) 021047


To see older, previously-approved labels, go to the "Approval History" section of this page. Older labels are for historical information only and should not be used for clinical purposes.
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
10/23/2001 002Manufacturing Change or Addition  
7/21/2000 001Labeling Revision Review 
8/27/1999 000Approval Letter
Label
Review 
 
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