Visitor Monitoring Drug History: NARDIL
 
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Label and Approval History

Drug Name: NARDIL
FDA Application No: (NDA) 011909
Active Ingredient(s): PHENELZINE SULFATE
Company: PARKE DAVIS
 
Label History
 
View the label approved on August 3, 2007 for NARDIL, (NDA) 011909


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
8/2/2007 038Labeling Revision Letter
Label 
2/6/2007 036Package Change Letter
Label 
2/18/2005 035Labeling Revision Letter 
9/2/2003 033Labeling Revision Letter
Label 
1/3/2002 030Labeling Revision  
2/25/1998 028Expiration Date Change  
2/24/1998 027Manufacturing Change or Addition  
7/14/1994 023Formulation Revision  
3/28/1985 013Labeling Revision  
11/3/1982 012Labeling Revision  
8/27/1986 010Control Supplement  
3/8/1978 009Labeling Revision  
8/27/1986 008Manufacturing Change or Addition  
6/9/1961 000Approval Other Important Information from FDA 
 
There are no Therapeutic Equivalents
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