DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
EMETE-CON
FDA Application No:
(NDA) 016820
Active Ingredient(s):
BENZQUINAMIDE HYDROCHLORIDE
Company:
PFIZER
Label History
Labels are not available on this site for EMETECON, (NDA) 016820
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
1/16/1990
015
Manufacturing Change or Addition
4/19/1989
014
Control Supplement
11/25/1986
013
Control Supplement
6/23/1983
011
Manufacturing Change or Addition
4/16/1981
010
Expiration Date Change
10/2/1979
009
Control Supplement
10/2/1979
008
Control Supplement
10/2/1979
007
Control Supplement
12/14/1977
006
Labeling Revision
12/14/1977
005
Formulation Revision
8/14/1974
003
Control Supplement
5/21/1974
002
Control Supplement
8/6/1974
001
Control Supplement
3/12/1974
000
Approval
There are no Therapeutic Equivalents
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