Visitor Monitoring Drug History: MANNITOL 20%
 
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Label and Approval History

Drug Name: MANNITOL 20%
FDA Application No: (NDA) 016269
Active Ingredient(s): MANNITOL
Company: HOSPIRA
 
Label History
 
Labels are not available on this site for MANNITOL 20, (NDA) 016269
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
11/18/2002 043Expiration Date Change  
9/5/2002 041Labeling  
1/17/1997 040Chemistry  
8/14/1995 039Chemistry  
8/27/1996 038Chemistry  
8/25/1994 037Labeling  
6/4/1991 036Chemistry  
2/1/1988 035Chemistry  
11/22/1985 033Chemistry  
7/5/1983 032Chemistry  
5/5/1982 031Labeling  
9/1/1981 030Labeling  
2/2/1981 029Chemistry  
10/4/1982 028Chemistry  
6/17/1982 027Labeling  
1/13/1981 026Chemistry  
9/25/1980 025Chemistry  
10/2/1980 024Labeling  
9/3/1980 023Chemistry  
6/10/1980 022Chemistry  
6/6/1980 021Chemistry  
5/27/1980 020Chemistry  
1/8/1980 019Chemistry  
7/22/1980 018Labeling  
7/22/1980 017Chemistry  
8/18/1978 016Chemistry  
12/2/1977 015Chemistry  
9/7/1978 014Chemistry  
2/4/1977 013Chemistry  
3/1/1976 012Chemistry  
12/22/1967 000Approval  
 
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