Visitor Monitoring Drug History: HEPARIN SODIUM 25,000 UNITS AND DEXTROSE 5% IN PLASTIC CONTAINER
 
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Label and Approval History

Drug Name: HEPARIN SODIUM 25,000 UNITS AND DEXTROSE 5% IN PLASTIC CONTAINER
FDA Application No: (NDA) 018814
Active Ingredient(s): HEPARIN SODIUM
Company: BAXTER HLTHCARE
 
Label History
 
Labels are not available on this site for HEPARIN SODIUM 25,000 UNITS AND DEXTROSE 5 IN PLASTIC CONTAINER, (NDA) 018814
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
11/23/1999 027Package Change  
10/19/2000 026Labeling Revision  
6/1/1999 025Manufacturing Change or Addition  
2/4/2000 024Labeling Revision  
9/17/1996 022Labeling Revision  
3/10/1994 021Control Supplement  
9/14/1994 020Manufacturing Change or Addition  
7/20/1994 019Formulation Revision  
7/20/1994 018Package Change  
4/15/1993 017Manufacturing Change or Addition  
7/16/1991 015Manufacturing Change or Addition  
11/19/1992 013Labeling Revision  
3/4/1991 012Control Supplement  
4/25/1991 011Control Supplement  
8/24/1989 010Control Supplement  
2/19/1988 009Labeling Revision  
7/8/1987 008Package Change  
10/8/1985 007Control Supplement  
7/9/1985 006General Efficacy (MarkIV)  
6/17/1985 005Package Change  
1/31/1985 004Labeling Revision  
10/16/1984 002Control Supplement  
6/8/1984 001Control Supplement  
10/31/1983 000Approval  
 
Therapeutic Equivalents
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