Visitor Monitoring Drug History: SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
 
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Label and Approval History

Drug Name: SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
FDA Application No: (NDA) 016733
Active Ingredient(s): SODIUM CHLORIDE
Company: B BRAUN
 
Label History
 
Labels are not available on this site for SODIUM CHLORIDE 0.9 IN PLASTIC CONTAINER, (NDA) 016733
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
10/20/2006 049Labeling Revision Letter 
7/8/2002 047Control Supplement  
4/3/2002 046Control Supplement  
4/12/2000 045Control Supplement  
3/25/1998 044Control Supplement  
9/11/1990 043Package Change  
4/19/1988 041Control Supplement  
10/10/1985 039Labeling Revision  
4/15/1985 038Labeling Revision  
3/5/1987 037Control Supplement  
4/3/1985 036Control Supplement  
5/17/1985 035Package Change  
5/24/1985 033Control Supplement  
9/24/1981 032Package Change  
9/28/1981 031Control Supplement  
3/12/1982 030Labeling Revision  
11/6/1981 029Manufacturing Change or Addition  
3/18/1981 028Control Supplement  
10/27/1981 027Labeling Revision  
10/27/1981 026Control Supplement  
7/16/1980 025Control Supplement  
2/15/1980 024Control Supplement  
9/25/1979 023Labeling Revision  
9/24/1979 022Control Supplement  
8/6/1979 021Labeling Revision  
1/4/1980 020Labeling Revision  
4/26/1979 019Control Supplement  
8/4/1978 018Control Supplement  
10/27/1978 017Control Supplement  
10/27/1978 016Control Supplement  
12/27/1978 015Labeling Revision  
12/27/1978 014Control Supplement  
5/26/1978 013Control Supplement  
3/15/1978 012Manufacturing Change or Addition  
3/30/1978 011Labeling Revision  
2/14/1978 010Control Supplement  
6/28/1977 009Control Supplement  
2/4/1977 008Control Supplement  
10/20/1976 007Labeling Revision  
4/2/1976 006Control Supplement  
4/2/1976 005Control Supplement  
4/2/1976 004Control Supplement  
8/30/1974 003Labeling Revision  
8/12/1970 000Approval  
 
Therapeutic Equivalents
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