Visitor Monitoring Drug History: HEPARIN SODIUM 2,000 UNITS AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
 
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Label and Approval History

Drug Name: HEPARIN SODIUM 2,000 UNITS AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
FDA Application No: (NDA) 018609
Active Ingredient(s): HEPARIN SODIUM
Company: BAXTER HLTHCARE
 
Label History
 
View the label approved on April 14, 2003 for HEPARIN SODIUM 2,000 UNITS AND SODIUM CHLORIDE 0.9 IN PLASTIC CONTAINER, (NDA) 018609


To see older, previously-approved labels, go to the "Approval History" section of this page. Older labels are for historical information only and should not be used for clinical purposes.
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
8/14/2001 037Control Supplement  
11/23/1999 036Package Change  
8/21/2001 035Labeling Revision Label 
6/1/1999 034Manufacturing Change or Addition  
8/21/2001 033Labeling Revision Label 
5/20/1997 032Package Change  
9/17/1996 031Labeling Revision  
3/10/1994 030Control Supplement  
9/14/1994 029Manufacturing Change or Addition  
4/15/1993 027Manufacturing Change or Addition  
3/4/1991 025Control Supplement  
7/26/1990 024Control Supplement  
2/1/1991 023Package Change  
8/24/1989 022Control Supplement  
11/8/1989 021Labeling Revision  
4/29/1987 020Package Change  
12/1/1986 019Control Supplement  
12/1/1986 018Control Supplement  
9/20/1985 017Control Supplement  
9/20/1985 016Package Change  
11/8/1989 015Labeling Revision  
10/16/1984 014Control Supplement  
8/3/1984 013Manufacturing Change or Addition  
2/28/1984 012Control Supplement  
3/6/1984 011Labeling Revision  
11/8/1989 010Practioner Draft Labeling  
3/6/1984 009Control Supplement  
3/6/1984 008Package Change  
3/6/1984 004Package Change  
8/9/1982 003Package Change  
8/9/1982 002Control Supplement  
6/29/1982 001Expiration Date Change  
4/28/1982 000Approval  
 
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