Visitor Monitoring Drug History: SELEGILINE HYDROCHLORIDE
 
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Label and Approval History

Drug Name: SELEGILINE HYDROCHLORIDE
FDA Application No: (NDA) 019334
Active Ingredient(s): SELEGILINE HYDROCHLORIDE
Company: SOMERSET
 
Label History
 
Labels are not available on this site for SELEGILINE HYDROCHLORIDE, (NDA) 019334
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
8/6/1997 017Labeling Revision  
7/13/1994 012Control Supplement  
2/12/1993 011Control Supplement  
1/5/1993 009Manufacturing Change or Addition  
1/5/1993 008Control Supplement  
1/5/1993 007Labeling Revision  
1/5/1993 006Manufacturing Change or Addition  
1/5/1993 005Labeling Revision  
7/25/1990 003Labeling Revision  
3/1/1990 002Package Change  
3/26/1990 001Labeling Revision  
6/5/1989 000Approval  
 
Therapeutic Equivalents
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