DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
TENUATE
FDA Application No:
(NDA) 017669
Active Ingredient(s):
DIETHYLPROPION HYDROCHLORIDE
Company:
SANOFI AVENTIS US
Label History
Labels are not available on this site for TENUATE, (NDA) 017669
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
5/18/1981
009
Labeling Revision
11/2/1979
008
Control Supplement
4/27/1978
007
Package Change
9/28/1976
004
Package Change
9/28/1976
003
Package Change
6/19/1975
001
Control Supplement
3/20/1975
000
Approval
Therapeutic Equivalents
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