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) 072579
Active Ingredient(s):
NIFEDIPINE
Company:
ACTAVIS ELIZABETH
Label History
Labels are not available on this site for NIFEDIPINE, (ANDA) 072579
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
1/6/2003
020
Control Supplement
8/20/2002
019
Labeling
8/22/2001
017
Labeling
11/2/2001
016
Control Supplement
1/24/2000
015
Package Change
2/9/1998
014
Labeling
10/1/1997
013
Labeling
10/18/1996
012
Labeling
8/28/1996
011
Labeling
4/22/1996
010
Labeling
1/18/1996
009
Chemistry
8/10/1992
007
Labeling
7/14/1992
006
Labeling in Effect
3/24/1992
005
Labeling in Effect
2/11/1992
004
Labeling
3/18/1992
003
Chemistry
5/12/1992
002
Labeling
4/28/1989
000
Approval
Therapeutic Equivalents
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