DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
HEPARIN SODIUM 12,500 UNITS IN SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER
FDA Application No:
(NDA) 019802
Active Ingredient(s):
HEPARIN SODIUM
Company:
B BRAUN
Label History
Labels are not available on this site for HEPARIN SODIUM 12,500 UNITS IN SODIUM CHLORIDE 0.45 IN PLASTIC CONTAINER, (NDA) 019802
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
7/12/2002
009
Control Supplement
2/15/2002
007
Package Change
11/22/2000
006
Control Supplement
6/5/1998
005
Control Supplement
12/22/1992
003
Labeling Revision
12/2/1992
002
Manufacturing Change or Addition
3/29/1993
001
Package Change
7/20/1992
000
Approval
Therapeutic Equivalents
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