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

Drug Name: MANNITOL 20%
FDA Application No: (NDA) 014738
Active Ingredient(s): MANNITOL
Company: B BRAUN
 
Label History
 
Labels are not available on this site for MANNITOL 20, (NDA) 014738
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
10/7/2002 015Microbiology  
5/16/1985 013Labeling  
4/6/1985 012Chemistry  
7/9/1984 009Chemistry  
5/4/1981 008Chemistry  
9/11/1981 007Labeling  
5/24/1982 006Labeling  
5/28/1981 005Chemistry  
5/2/1979 004Chemistry  
8/10/1977 003Labeling  
7/30/1964 000Approval  
 
Therapeutic Equivalents
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