Visitor Monitoring Drug History: SODIUM CHLORIDE
 
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Label and Approval History

Drug Name: SODIUM CHLORIDE
FDA Application No: (NDA) 017013
Active Ingredient(s): SODIUM CHLORIDE
Company: ABBOTT
 
Label History
 
Labels are not available on this site for SODIUM CHLORIDE, (NDA) 017013
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
8/27/1996 018Control Supplement  
11/16/1982 016Control Supplement  
6/9/1982 015Manufacturing Change or Addition  
4/21/1982 013Labeling Revision  
12/11/1980 010Package Change  
8/12/1981 009Labeling Revision  
1/19/1979 007Manufacturing Change or Addition  
1/8/1979 006Control Supplement  
4/18/1979 004Labeling Revision  
9/27/1976 003Control Supplement  
9/14/1976 002Control Supplement  
10/8/1971 000Approval  
 
Therapeutic Equivalents
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