Visitor Monitoring Drug History: HEPARIN SODIUM
 
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Label and Approval History

Drug Name: HEPARIN SODIUM
FDA Application No: (NDA) 017007
Active Ingredient(s): HEPARIN SODIUM
Company: BAXTER HLTHCARE CORP
 
Label History
 
Labels are not available on this site for HEPARIN SODIUM, (NDA) 017007
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
9/6/2000 038Labeling Revision  
3/5/1997 036Labeling Revision  
5/20/1996 035Package Change  
10/20/1993 033Package Change  
6/14/1993 032Package Change  
7/20/1990 031Labeling Revision  
7/13/1989 029Labeling Revision  
6/29/1989 028Labeling Revision  
2/28/1991 025Control Supplement  
7/29/1987 024Package Change  
4/14/1987 023Package Change  
3/5/1987 022Labeling Revision  
10/19/1983 019Labeling Revision  
8/29/1983 018Labeling Revision  
5/25/1983 017Package Change  
7/30/1982 016Expiration Date Change  
4/7/1986 015Practioner Draft Labeling  
5/14/1981 014Control Supplement  
7/2/1980 013Control Supplement  
7/2/1980 012Control Supplement  
10/4/1978 011Labeling Revision  
7/3/1978 010Labeling Revision  
7/3/1978 009Control Supplement  
2/2/1978 008Control Supplement  
2/2/1978 007Control Supplement  
12/29/1976 006Package Change  
10/17/1975 005Control Supplement  
12/12/1975 004Control Supplement  
3/28/1975 003Control Supplement  
5/28/1974 000Approval  
 
Therapeutic Equivalents
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