DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
RADIONUCLIDE-LABELED (125 I) FIBRINOGEN (HUMAN) SENSOR
FDA Application No:
(NDA) 017787
Active Ingredient(s):
FIBRINOGEN, I-125
Company:
ABBOTT
Label History
Labels are not available on this site for RADIONUCLIDELABELED (125 I) FIBRINOGEN (HUMAN) SENSOR, (NDA) 017787
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
3/7/1979
008
Manufacturing Change or Addition
11/16/1978
006
Labeling Revision
3/3/1978
005
Control Supplement
3/7/1978
004
Control Supplement
6/28/1976
000
Approval
There are no Therapeutic Equivalents
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