DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
TECHNETIUM TC 99M HSA
FDA Application No:
(NDA) 017775
Active Ingredient(s):
TECHNETIUM TC-99M ALBUMIN KIT
Company:
GE HEALTHCARE
Label History
Labels are not available on this site for TECHNETIUM TC 99M HSA, (NDA) 017775
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
11/25/2002
023
Control Supplement
4/10/2001
022
Manufacturing Change or Addition
9/29/2000
021
Manufacturing Change or Addition
11/12/1999
020
Control Supplement
2/9/1994
019
Manufacturing Change or Addition
12/15/1989
018
Labeling Revision
2/17/1989
017
Control Supplement
12/23/1988
016
Manufacturing Change or Addition
6/25/1986
015
Labeling Revision
4/19/1985
013
Labeling Revision
3/22/1982
011
Labeling Revision
5/13/1982
010
Labeling Revision
3/22/1982
009
Labeling Revision
3/22/1982
006
Labeling Revision
3/22/1982
005
Labeling Revision
4/1/1977
000
Approval
There are no Therapeutic Equivalents
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