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) 019953
Active Ingredient(s): HEPARIN SODIUM
Company: B BRAUN
 
Label History
 
Labels are not available on this site for HEPARIN SODIUM 1,000 UNITS IN SODIUM CHLORIDE 0.9 IN PLASTIC CONTAINER, (NDA) 019953
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
4/13/2004 012Labeling Revision Letter 
7/12/2002 011Control Supplement  
2/15/2002 009Package Change  
11/22/2000 008Control Supplement  
3/1/2000 007Control Supplement  
6/5/1998 006Control Supplement  
7/30/1996 005Manufacturing Change or Addition  
3/9/1995 004Control Supplement  
12/22/1992 003Labeling Revision  
12/2/1992 002Manufacturing Change or Addition  
3/29/1993 001Package Change  
7/20/1992 000Approval  
 
Therapeutic Equivalents
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