DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
VERAPAMIL HYDROCHLORIDE
FDA Application No:
(ANDA) 071019
Active Ingredient(s):
VERAPAMIL HYDROCHLORIDE
Company:
ACTAVIS ELIZABETH
Label History
Labels are not available on this site for VERAPAMIL HYDROCHLORIDE, (ANDA) 071019
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
11/2/2001
037
Control Supplement
9/18/2000
036
Control Supplement
4/21/2000
035
Package Change
8/5/1998
034
Labeling
5/8/1996
033
Chemistry
5/8/1996
032
Chemistry
1/18/1996
031
Chemistry
7/25/1994
030
Chemistry
1/9/1992
029
Labeling
11/27/1991
028
Labeling
6/5/1992
027
Chemistry
6/5/1992
026
Chemistry
10/4/1991
025
Labeling
3/19/1993
024
Chemistry
3/19/1993
023
Chemistry
12/15/1988
019
SBA
4/7/1989
019
Chemistry
4/7/1989
018
Chemistry
4/7/1989
017
Chemistry
6/19/1989
016
Labeling
11/7/1988
015
Chemistry
6/15/1988
014
Chemistry
4/21/1989
013
Chemistry
6/15/1988
012
Chemistry
6/15/1988
011
Chemistry
5/21/1987
008
Chemistry
5/21/1987
007
Chemistry
5/21/1987
006
Chemistry
5/21/1987
005
Chemistry
12/24/1986
001
Chemistry
9/23/1986
000
Approval
Therapeutic Equivalents
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