DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
ADALAT
FDA Application No:
(NDA) 019478
Active Ingredient(s):
NIFEDIPINE
Company:
BAYER PHARMS
Label History
Labels are not available on this site for ADALAT, (NDA) 019478
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
12/22/1997
012
Package Change
3/22/1996
011
Labeling Revision
9/22/1993
010
Labeling Revision
1/23/1992
009
Labeling Revision
9/13/1991
008
Labeling Revision
9/13/1991
007
Labeling Revision
11/21/1989
006
Labeling Revision
8/10/1989
005
Control Supplement
10/26/1988
004
Formulation Revision
7/21/1988
003
Package Change
10/7/1986
002
Expiration Date Change
9/17/1986
001
Labeling Revision
11/27/1985
000
Approval
Therapeutic Equivalents
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