Visitor Monitoring Drug History: MANNITOL 15% W/ DEXTROSE 5% IN SODIUM CHLORIDE 0.45%
 
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Label and Approval History

Drug Name: MANNITOL 15% W/ DEXTROSE 5% IN SODIUM CHLORIDE 0.45%
FDA Application No: (NDA) 016080
Active Ingredient(s): MANNITOL
Company: B BRAUN
 
Label History
 
Labels are not available on this site for MANNITOL 15 W DEXTROSE 5 IN SODIUM CHLORIDE 0.45, (NDA) 016080
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
5/24/1985 014Labeling Revision  
5/16/1985 013Labeling Revision  
4/6/1985 012Package Change  
7/9/1984 009Control Supplement  
5/4/1981 008Control Supplement  
9/11/1981 007Labeling Revision  
5/24/1982 006Practioner Draft Labeling  
12/17/1981 005Manufacturing Change or Addition  
5/1/1979 004Control Supplement  
8/8/1977 003Labeling Revision  
10/8/1965 000Approval  
 
Therapeutic Equivalents
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