DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
HEPARIN SODIUM 25,000 UNITS IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
FDA Application No:
(NDA) 019135
Active Ingredient(s):
HEPARIN SODIUM
Company:
B BRAUN
Label History
Labels are not available on this site for HEPARIN SODIUM 25,000 UNITS IN SODIUM CHLORIDE 0.9 IN PLASTIC CONTAINER, (NDA) 019135
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
3/30/1990
005
Package Change
11/22/1988
004
Labeling Revision
10/21/1986
002
Control Supplement
9/10/1985
001
Package Change
3/29/1985
000
Approval
Therapeutic Equivalents
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