Visitor Monitoring Drug History: HEPARIN SODIUM 1,000 UNITS IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
 
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Label and Approval History

Drug Name: HEPARIN SODIUM 1,000 UNITS IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
FDA Application No: (NDA) 018916
Active Ingredient(s): HEPARIN SODIUM
Company: HOSPIRA
 
Label History
 
Labels are not available on this site for HEPARIN SODIUM 1,000 UNITS IN SODIUM CHLORIDE 0.9 IN PLASTIC CONTAINER, (NDA) 018916
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
11/19/1999 033Labeling Revision  
10/27/1998 032Control Supplement  
8/29/1997 031Package Change  
6/25/1997 030Manufacturing Change or Addition  
6/9/1997 029Manufacturing Change or Addition  
8/25/1998 028Labeling Revision  
4/3/1997 027Manufacturing Change or Addition  
8/29/1996 026Package Change  
2/7/1996 025Package Change  
9/5/1996 024Manufacturing Change or Addition  
8/30/1996 023Manufacturing Change or Addition  
10/2/1991 021Labeling Revision  
2/25/1992 020Manufacturing Change or Addition  
2/18/1992 018Package Change  
10/29/1990 016Control Supplement  
2/16/1990 015Control Supplement  
10/24/1988 012Labeling Revision  
6/23/1989 008New Dosage Regimen  
8/21/1987 007Package Change  
10/29/1986 006Formulation Revision  
8/8/1986 005Manufacturing Change or Addition  
10/29/1985 004Formulation Revision  
10/29/1985 003Formulation Revision  
4/16/1985 002Package Change  
9/24/1984 001Labeling Revision  
1/31/1984 000Approval  
 
Therapeutic Equivalents
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