Visitor Monitoring Drug History: HEP-LOCK U/P
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
Browse by Letter: A B C D E F G H I J K L M N O P Q R S T U V W X Y Z 0-9
Label and Approval History

Drug Name: HEP-LOCK U/P
FDA Application No: (NDA) 017037
Active Ingredient(s): HEPARIN SODIUM
Company: BAXTER HLTHCARE
 
Label History
 
View the label approved on October 5, 2006 for HEPLOCK UP, (NDA) 017037


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
10/4/2006 158Labeling Revision Letter
Label 
9/2/2005 156Package Change Letter
Label 
9/2/2005 155Formulation Revision Letter
Label 
9/2/2005 154Control Supplement Letter
Label 
11/22/2002 151Expiration Date Change  
11/25/2002 150Expiration Date Change  
11/21/2002 149Package Change  
11/22/2002 148Package Change  
7/15/2002 147Expiration Date Change  
2/5/2002 146Labeling Revision  
8/31/2001 145Control Supplement  
11/16/2000 144Package Change  
5/31/2000 143Control Supplement  
5/26/2000 142Control Supplement  
5/26/2000 141Control Supplement  
5/1/2000 140Control Supplement  
2/15/2000 139Control Supplement  
5/13/1999 138Control Supplement  
9/30/1999 136Labeling Revision  
2/20/1998 134Control Supplement  
6/23/1998 133Labeling Revision  
4/24/1997 132Manufacturing Change or Addition  
3/5/1996 131Control Supplement  
2/9/1993 130Control Supplement  
4/23/1991 128Labeling Revision  
9/27/1989 127Expiration Date Change  
6/20/1989 126Labeling Revision  
6/20/1989 125Labeling Revision  
6/28/1989 124Labeling Revision  
10/14/1987 123Labeling Revision  
9/16/1987 122Labeling Revision  
7/2/1987 121Labeling Revision  
7/2/1987 120Labeling Revision  
4/24/1987 119Control Supplement  
3/10/1987 118Manufacturing Change or Addition  
4/29/1987 117Expiration Date Change  
9/23/1986 116Manufacturing Change or Addition  
4/29/1987 115Labeling Revision  
1/30/1986 114Labeling Revision  
10/10/1985 113Manufacturing Change or Addition  
4/7/1986 112Package Change  
8/29/1985 111Package Change  
8/29/1985 110Package Change  
5/13/1985 109Labeling Revision  
1/21/1986 108Formulation Revision  
10/11/1984 107Labeling Revision  
10/11/1984 105Labeling Revision  
8/2/1984 104Formulation Revision  
12/21/1983 102Labeling Revision  
9/5/1983 101Labeling Revision  
6/10/1983 100Control Supplement  
9/13/1983 099Control Supplement  
10/6/1982 098Manufacturing Change or Addition  
8/18/1982 097Package Change  
6/4/1982 096Manufacturing Change or Addition  
11/20/1981 095Labeling Revision  
5/22/1981 094Labeling Revision  
1/21/1980 093Control Supplement  
9/25/1979 092Formulation Revision  
3/6/1979 091Control Supplement  
1/16/1979 090Control Supplement  
1/16/1979 089Control Supplement  
1/16/1979 088Labeling Revision  
10/4/1978 087Labeling Revision  
8/4/1978 086Control Supplement  
7/31/1978 085Labeling Revision  
8/4/1978 084Manufacturing Change or Addition  
7/31/1978 083Manufacturing Change or Addition  
7/31/1978 082Labeling Revision  
12/14/1977 081Labeling Revision  
12/14/1977 080Manufacturing Change or Addition  
12/14/1977 079Labeling Revision  
4/27/1978 078Control Supplement  
4/27/1978 077Labeling Revision  
12/14/1977 075Labeling Revision  
12/14/1977 074Formulation Revision  
1/3/1978 073Manufacturing Change or Addition  
8/2/1977 072Distributor  
5/26/1977 071Control Supplement  
4/26/1977 070Package Change  
5/26/1977 069Package Change  
2/17/1977 067Control Supplement  
10/19/1976 066Distributor  
10/19/1976 065Labeling Revision  
9/8/1976 063Control Supplement  
9/8/1976 059Control Supplement  
9/8/1976 058Control Supplement  
9/8/1976 057Control Supplement  
5/28/1976 055Control Supplement  
1/9/1976 048Control Supplement  
9/4/1975 047Labeling Revision  
9/4/1975 046Labeling Revision  
9/4/1975 045Distributor  
9/4/1975 044Labeling Revision  
9/4/1975 043Labeling Revision  
9/4/1975 042Labeling Revision  
4/23/1975 039Control Supplement  
3/24/1975 038Labeling Revision  
3/5/1984 013Labeling Revision  
3/22/1972 000Approval  
 
Therapeutic Equivalents
©2019 Drugs That Causes a False Positive on a Drug Test