DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
WYAMINE SULFATE
FDA Application No:
(NDA) 008248
Active Ingredient(s):
MEPHENTERMINE SULFATE
Company:
BAXTER HLTHCARE CORP
Label History
Labels are not available on this site for WYAMINE SULFATE, (NDA) 008248
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
5/31/1988
007
Labeling Revision
10/23/1985
006
Control Supplement
2/17/1993
005
Practioner Draft Labeling
6/7/1978
004
Control Supplement
12/29/1951
000
Approval
There are no Therapeutic Equivalents
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