DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
INDERIDE LA 120/50
FDA Application No:
(NDA) 019059
Active Ingredient(s):
HYDROCHLOROTHIAZIDE; PROPRANOLOL HYDROCHLORIDE
Company:
WYETH AYERST
Label History
Labels are not available on this site for INDERIDE LA 12050, (NDA) 019059
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
5/3/2001
017
Labeling Revision
11/1/2001
016
Labeling Revision
5/8/1998
015
Labeling Revision
5/14/1990
014
Expiration Date Change
4/12/1989
013
Package Change
4/10/1989
012
Control Supplement
1/25/1989
011
Control Supplement
5/25/1988
010
Package Change
1/6/1987
009
Expiration Date Change
11/12/1986
008
Manufacturing Change or Addition
1/20/1987
007
Formulation Revision
7/2/1986
005
Manufacturing Change or Addition
3/20/1986
004
Control Supplement
3/20/1986
003
Expiration Date Change
7/24/1986
002
Manufacturing Change or Addition
10/22/1985
001
Formulation Revision
7/3/1985
000
Approval
There are no Therapeutic Equivalents
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