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 MAA
FDA Application No:
(NDA) 017773
Active Ingredient(s):
TECHNETIUM TC-99M ALBUMIN AGGREGATED KIT
Company:
GE HEALTHCARE
Label History
Labels are not available on this site for TECHNETIUM TC 99M MAA, (NDA) 017773
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
7/6/1989
017
Labeling Revision
2/17/1989
016
Control Supplement
12/28/1988
015
Manufacturing Change or Addition
6/3/1988
014
Manufacturing Change or Addition
5/22/1985
012
Labeling Revision
4/14/1982
010
Labeling Revision
3/31/1982
009
Manufacturing Change or Addition
4/28/1982
008
Practioner Draft Labeling
6/5/1978
003
Control Supplement
11/17/1977
001
Labeling Revision
11/16/1976
000
Approval
Therapeutic Equivalents
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