DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
CARDIOGRAFIN
FDA Application No:
(NDA) 011620
Active Ingredient(s):
DIATRIZOATE MEGLUMINE
Company:
BRACCO
Label History
Labels are not available on this site for CARDIOGRAFIN, (NDA) 011620
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
1/28/1985
026
Manufacturing Change or Addition
7/11/1985
024
Manufacturing Change or Addition
8/5/1982
022
Labeling Revision
7/29/1980
021
Control Supplement
11/27/1978
018
Manufacturing Change or Addition
2/27/1978
017
Control Supplement
9/13/1978
016
Control Supplement
3/30/1977
015
Control Supplement
1/11/1977
013
Control Supplement
12/6/1976
012
Labeling Revision
9/14/1976
011
Expiration Date Change
5/10/1976
010
Control Supplement
9/24/1975
009
Control Supplement
12/3/1958
000
Approval
There are no Therapeutic Equivalents
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