DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
GASTROGRAFIN
FDA Application No:
(NDA) 011245
Active Ingredient(s):
DIATRIZOATE MEGLUMINE; DIATRIZOATE SODIUM
Company:
BRACCO
Label History
Labels are not available on this site for GASTROGRAFIN, (NDA) 011245
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
8/29/2005
032
Control Supplement
Letter
12/15/2000
030
Manufacturing Change or Addition
8/5/1994
029
Labeling Revision
5/19/1994
028
Manufacturing Change or Addition
3/5/1991
027
Package Change
1/28/1985
026
Manufacturing Change or Addition
9/14/1983
023
Practioner Draft Labeling
8/3/1983
022
Package Change
2/2/1983
021
Labeling Revision
9/14/1983
020
General Efficacy (MarkIV)
9/13/1979
019
Labeling Revision
12/28/1978
018
Formulation Revision
2/27/1978
017
Control Supplement
9/16/1978
016
Control Supplement
9/25/1975
013
Control Supplement
9/8/1976
012
Labeling Revision
1/17/1958
000
Approval
There are no Therapeutic Equivalents
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