DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
TENSILON
FDA Application No:
(NDA) 007959
Active Ingredient(s):
EDROPHONIUM CHLORIDE
Company:
VALEANT PHARM INTL
Label History
Labels are not available on this site for TENSILON, (NDA) 007959
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
2/26/2003
015
Labeling Revision
Letter
10/1/1997
014
Control Supplement
4/24/2002
013
Labeling Revision
Letter
8/9/1993
012
Package Change
1/3/1986
008
Manufacturing Change or Addition
3/7/1985
007
Manufacturing Change or Addition
4/5/1983
006
Labeling Revision
5/3/1951
000
Approval
Therapeutic Equivalents
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