DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
NIFEDIPINE
FDA Application No:
(ANDA) 072556
Active Ingredient(s):
NIFEDIPINE
Company:
ACTAVIS ELIZABETH
Label History
Labels are not available on this site for NIFEDIPINE, (ANDA) 072556
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
2/8/2007
028
Control Supplement
1/6/2003
021
Control Supplement
8/20/2002
020
Labeling
8/22/2001
018
Labeling
11/2/2001
017
Control Supplement
2/9/1998
016
Labeling
10/1/1997
015
Labeling
10/18/1996
014
Labeling
8/28/1996
013
Labeling
4/22/1996
012
Labeling
1/18/1996
011
Chemistry
8/10/1992
009
Labeling
7/14/1992
008
Labeling in Effect
3/24/1992
007
Labeling in Effect
2/11/1992
006
Labeling
1/22/1992
005
Chemistry
1/22/1992
004
Chemistry
11/28/1990
002
Labeling
4/28/1989
000
Approval
Therapeutic Equivalents
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