Visitor Monitoring Drug History: HEP FLUSH KIT IN PLASTIC CONTAINER
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
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Label and Approval History

Drug Name: HEP FLUSH KIT IN PLASTIC CONTAINER
FDA Application No: (NDA) 017029
Active Ingredient(s): HEPARIN SODIUM
Company: ABRAXIS PHARM
 
Label History
 
Labels are not available on this site for HEP FLUSH KIT IN PLASTIC CONTAINER, (NDA) 017029
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
3/22/2002 099Labeling Revision Letter 
12/13/1999 098Manufacturing Change or Addition  
3/8/2000 097Package Change  
11/4/1997 096Control Supplement  
6/24/1997 095Control Supplement  
8/6/1998 094Manufacturing Change or Addition  
5/17/1995 084Manufacturing Change or Addition  
10/27/1994 078Manufacturing Change or Addition  
7/26/1996 073Control Supplement  
8/25/1993 069Labeling Revision  
8/6/1998 063Manufacturing Change or Addition  
8/6/1998 062Manufacturing Change or Addition  
6/8/1989 061Package Change  
9/22/1988 060Labeling Revision  
2/16/1988 058Control Supplement  
12/1/1989 057Package Change  
6/26/1992 056Labeling Revision  
4/28/1986 054Control Supplement  
4/7/1986 053Labeling Revision  
9/22/1987 051Package Change  
9/22/1987 050Package Change  
7/29/1985 049General Efficacy (MarkIV)  
11/6/1984 048Package Change  
12/5/1985 047Package Change  
12/5/1985 046Package Change  
12/5/1985 045Package Change  
12/5/1985 044Package Change  
12/5/1985 043Package Change  
12/5/1985 042Package Change  
11/2/1983 041Formulation Revision  
11/2/1983 040Formulation Revision  
11/2/1983 039Formulation Revision  
11/2/1983 038Formulation Revision  
5/16/1985 037Formulation Revision  
11/2/1983 036Formulation Revision  
11/2/1983 034Expiration Date Change  
1/4/1983 033Expiration Date Change  
9/21/1982 032Manufacturing Change or Addition  
9/21/1982 031Manufacturing Change or Addition  
5/6/1982 030Labeling Revision  
9/17/1982 029Control Supplement  
2/24/1981 027Labeling Revision  
3/24/1981 026Manufacturing Change or Addition  
10/31/1979 025Control Supplement  
10/31/1979 024Manufacturing Change or Addition  
11/21/1978 023Control Supplement  
11/21/1978 022Control Supplement  
5/23/1978 021Labeling Revision  
12/14/1977 020Control Supplement  
12/3/1976 019Control Supplement  
12/3/1976 017Formulation Revision  
1/26/1977 016Formulation Revision  
12/4/1977 015Labeling Revision  
6/16/1976 014Manufacturing Change or Addition  
2/9/1976 012Labeling Revision  
1/9/1976 011Control Supplement  
1/9/1976 010Formulation Revision  
3/17/1976 009Control Supplement  
2/9/1976 008Control Supplement  
8/29/1975 007Control Supplement  
2/22/1972 000Approval  
 
Therapeutic Equivalents
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