DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
HEPARIN SODIUM 20,000 UNITS IN DEXTROSE 5% IN PLASTIC CONTAINER
FDA Application No:
(NDA) 019952
Active Ingredient(s):
HEPARIN SODIUM
Company:
B BRAUN
Label History
Labels are not available on this site for HEPARIN SODIUM 20,000 UNITS IN DEXTROSE 5 IN PLASTIC CONTAINER, (NDA) 019952
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
4/13/2004
012
Labeling Revision
Letter
7/12/2002
010
Control Supplement
2/15/2002
008
Package Change
11/22/2000
007
Control Supplement
3/1/2000
006
Control Supplement
6/5/1998
005
Control Supplement
7/30/1996
004
Manufacturing Change or Addition
12/8/1994
003
Control Supplement
12/22/1992
002
Labeling Revision
3/29/1993
001
Package Change
7/20/1992
000
Approval
Therapeutic Equivalents
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