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 PENTETATE KIT
FDA Application No:
(NDA) 017264
Active Ingredient(s):
TECHNETIUM TC-99M PENTETATE KIT
Company:
GE HEALTHCARE
Label History
Labels are not available on this site for TECHNETIUM TC99M PENTETATE KIT, (NDA) 017264
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
2/17/1989
025
Control Supplement
12/23/1988
024
Manufacturing Change or Addition
9/27/1982
021
Labeling Revision
10/8/1982
020
Practioner Draft Labeling
8/15/1980
018
Labeling Revision
9/13/1979
014
Labeling Revision
9/13/1979
013
Labeling Revision
9/13/1979
012
Distributor
9/13/1979
011
Manufacturing Change or Addition
9/13/1979
009
Labeling Revision
4/26/1977
008
Control Supplement
1/30/1976
006
Control Supplement
4/26/1976
005
Control Supplement
9/19/1975
002
Control Supplement
2/14/1974
000
Approval
Therapeutic Equivalents
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