DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
VASCOR
FDA Application No:
(NDA) 019002
Active Ingredient(s):
BEPRIDIL HYDROCHLORIDE
Company:
JOHNSON AND JOHNSON
Label History
Labels are not available on this site for VASCOR, (NDA) 019002
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
2/6/2001
010
Manufacturing Change or Addition
7/12/2000
009
Labeling Revision
3/10/1998
007
Labeling Revision
6/28/1994
006
Manufacturing Change or Addition
1/28/1993
005
Manufacturing Change or Addition
1/28/1993
004
Labeling Revision
1/28/1993
003
Labeling Revision
5/12/1994
002
Control Supplement
Review
10/6/1993
001
Control Supplement
12/28/1990
000
Approval
Therapeutic Equivalents
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