DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
PHENERGAN
FDA Application No:
(NDA) 008857
Active Ingredient(s):
PROMETHAZINE HYDROCHLORIDE
Company:
WYETH AYERST
Label History
Labels are not available on this site for PHENERGAN, (NDA) 008857
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
8/16/1993
019
Package Change
9/21/1993
017
Package Change
2/26/1993
016
Manufacturing Change or Addition
6/30/1988
015
Control Supplement
5/6/1987
014
Labeling Revision
3/4/1987
013
Package Change
3/31/1987
012
Labeling Revision
2/27/1986
011
Control Supplement
5/29/1986
010
Control Supplement
9/18/1998
009
Practioner Draft Labeling
8/8/1979
008
Control Supplement
8/8/1979
007
Labeling Revision
10/30/1978
006
Labeling Revision
8/20/1956
000
Approval
There are no Therapeutic Equivalents
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