DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
HEPARIN SODIUM 10,000 UNITS IN SODIUM CHLORIDE 0.45%
FDA Application No:
(NDA) 018911
Active Ingredient(s):
HEPARIN SODIUM
Company:
HOSPIRA
Label History
Labels are not available on this site for HEPARIN SODIUM 10,000 UNITS IN SODIUM CHLORIDE 0.45, (NDA) 018911
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
8/24/1999
010
Labeling Revision
5/27/1998
009
Labeling Revision
8/24/1995
008
Manufacturing Change or Addition
8/29/1996
007
Control Supplement
2/25/1992
006
Manufacturing Change or Addition
7/24/1991
005
Labeling Revision
9/14/1987
003
Labeling Revision
9/24/1986
002
Manufacturing Change or Addition
7/29/1985
001
Labeling Revision
1/30/1985
000
Approval
Therapeutic Equivalents
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