Visitor Monitoring Drug History: PROPECIA
 
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: PROPECIA
FDA Application No: (NDA) 020788
Active Ingredient(s): FINASTERIDE
Company: MERCK
 
Label History
 
View the label approved on November 1, 2004 for PROPECIA, (NDA) 020788


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
10/21/2004 011Labeling Revision Letter
Label 
10/21/2004 010Labeling Revision Letter
Label 
10/30/2002 008Control Supplement  
4/10/2002 007Efficacy Supplement with Clinical Data to Support Letter
Label 
7/18/2000 006Expiration Date Change  
4/10/2002 005Labeling Revision Letter
Label 
4/10/2002 004Labeling Revision Letter
Label 
12/8/2001 003Labeling Revision Label 
10/21/2004 002Labeling Revision Letter
Label 
11/3/1998 001Control Supplement  
12/19/1997 000Approval Review 
 
Therapeutic Equivalents
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