DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
CALAN
FDA Application No:
(NDA) 018817
Active Ingredient(s):
VERAPAMIL HYDROCHLORIDE
Company:
GD SEARLE LLC
Label History
Labels are not available on this site for CALAN, (NDA) 018817
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
1/13/1998
019
Labeling Revision
5/14/1996
018
Manufacturing Change or Addition
2/7/1996
017
Package Change
11/4/1994
016
Labeling Revision
9/27/1991
015
Labeling Revision
8/12/1991
014
Labeling Revision
2/14/1990
013
Labeling Revision
4/13/1988
012
Practioner Draft Labeling
2/23/1988
011
Labeling Revision
4/29/1987
010
Labeling Revision
4/29/1987
009
Labeling Revision
4/29/1987
008
Control Supplement
2/23/1988
007
New Dosage Regimen
6/27/1986
006
Labeling Revision
5/6/1986
005
Control Supplement
10/20/1986
004
Control Supplement
12/16/1986
003
New or Modified Indication
6/4/1985
001
Formulation Revision
9/10/1984
000
Approval
Therapeutic Equivalents
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