DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
HEPARIN SODIUM 5,000 UNITS IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
FDA Application No:
(NDA) 019042
Active Ingredient(s):
HEPARIN SODIUM
Company:
B BRAUN
Label History
Labels are not available on this site for HEPARIN SODIUM 5,000 UNITS IN SODIUM CHLORIDE 0.9 IN PLASTIC CONTAINER, (NDA) 019042
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
4/20/1992
006
Manufacturing Change or Addition
3/30/1990
005
Package Change
6/21/1989
004
Labeling Revision
4/17/1987
002
Control Supplement
9/10/1985
001
Package Change
3/29/1985
000
Approval
Therapeutic Equivalents
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