DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
HEPARIN SODIUM
FDA Application No:
(NDA) 004570
Active Ingredient(s):
HEPARIN SODIUM
Company:
PHARMACIA AND UPJOHN
Label History
Labels are not available on this site for HEPARIN SODIUM, (NDA) 004570
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
4/3/2000
056
Manufacturing Change or Addition
9/15/1999
055
Labeling Revision
3/4/1996
054
Labeling Revision
1/31/1996
053
Manufacturing Change or Addition
7/9/1991
052
Control Supplement
11/16/1988
051
Labeling Revision
8/12/1988
050
Labeling Revision
1/29/1990
049
Control Supplement
7/24/1987
048
Labeling Revision
1/21/1987
047
Labeling Revision
1/29/1988
046
Control Supplement
3/25/1983
045
Labeling Revision
1/21/1983
044
Labeling Revision
10/24/1986
043
Practioner Draft Labeling
8/19/1981
042
Labeling Revision
6/2/1981
041
Labeling Revision
2/4/1981
040
Labeling Revision
1/14/1981
039
Labeling Revision
12/3/1980
038
Package Change
8/20/1980
037
Control Supplement
10/14/1980
036
Package Change
2/18/1981
035
Labeling Revision
2/5/1980
034
Formulation Revision
6/2/1981
033
Labeling Revision
2/5/1980
032
Control Supplement
2/5/1980
031
Package Change
10/4/1978
029
Control Supplement
2/2/1978
026
Control Supplement
2/11/1977
023
Formulation Revision
2/24/1976
022
Labeling Revision
2/24/1976
021
Labeling Revision
7/9/1976
020
Package Change
8/14/1975
019
Labeling Revision
8/14/1975
018
Control Supplement
2/5/1942
000
Approval
Therapeutic Equivalents
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