Visitor Monitoring Drug History: MANNITOL 25%
 
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Label and Approval History

Drug Name: MANNITOL 25%
FDA Application No: (ANDA) 080677
Active Ingredient(s): MANNITOL
Company: ABRAXIS PHARM
 
Label History
 
Labels are not available on this site for MANNITOL 25, (ANDA) 080677
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
7/14/1995 035Chemistry  
4/8/1993 034Labeling in Effect  
5/1/1992 033Labeling  
6/19/1991 032Labeling in Effect  
12/6/1994 031Chemistry in Effect  
8/13/1999 030Chemistry  
1/11/1989 029Chemistry  
1/11/1989 028Chemistry  
12/12/1985 026Chemistry  
10/18/1985 025Chemistry  
1/10/1985 023Chemistry  
9/20/1983 022Chemistry  
11/1/1982 020Chemistry  
11/8/1982 019Chemistry  
8/11/1972 000Approval  
 
Therapeutic Equivalents
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