DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
PROFERDEX
FDA Application No:
(NDA) 017807
Active Ingredient(s):
IRON DEXTRAN
Company:
NEW RIVER
Label History
Labels are not available on this site for PROFERDEX, (NDA) 017807
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
3/6/1989
007
Control Supplement
10/31/1986
006
Control Supplement
10/3/1984
005
Control Supplement
11/19/1984
004
Control Supplement
4/17/1986
003
Practioner Draft Labeling
1/4/1984
002
Package Change
11/5/1982
001
Labeling Revision
3/26/1981
000
Approval
Therapeutic Equivalents
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