DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
HIPPUTOPE
FDA Application No:
(NDA) 015419
Active Ingredient(s):
IODOHIPPURATE SODIUM, I-131
Company:
BRACCO
Label History
Labels are not available on this site for HIPPUTOPE, (NDA) 015419
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
9/30/1985
014
Manufacturing Change or Addition
6/12/1985
012
Practioner Draft Labeling
6/8/1983
009
Manufacturing Change or Addition
6/25/1970
000
Approval
There are no Therapeutic Equivalents
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