Visitor Monitoring Drug History: HYDROGENATED ERGOT ALKALOIDS
 
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Label and Approval History

Drug Name: HYDROGENATED ERGOT ALKALOIDS
FDA Application No: (ANDA) 087185
Active Ingredient(s): ERGOLOID MESYLATES
Company: IVAX PHARMS
 
Label History
 
Labels are not available on this site for HYDROGENATED ERGOT ALKALOIDS, (ANDA) 087185
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
7/29/2002 032Facility Addition  
3/12/2002 031Facility Addition  
6/27/2002 030Package Change  
7/21/2000 029Facility Addition  
7/21/2000 028Facility Addition  
1/28/2000 027Facility Addition  
11/23/1999 026Facility Addition  
8/20/1999 025Chemistry  
12/9/1998 024Chemistry  
5/30/1997 023Chemistry  
11/22/1995 022Chemistry  
8/24/1994 021Chemistry in Effect  
6/27/1995 019Chemistry in Effect  
5/17/1990 018Labeling  
8/2/1989 017Labeling  
2/11/1988 016Chemistry  
8/22/1988 015Chemistry  
2/11/1988 014Chemistry  
2/11/1988 013Chemistry  
11/20/1980 000Approval  
 
Therapeutic Equivalents
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