DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
OPTIPRANOLOL
FDA Application No:
(NDA) 019907
Active Ingredient(s):
METIPRANOLOL HYDROCHLORIDE
Company:
BAUSCH AND LOMB
Label History
Labels are not available on this site for OPTIPRANOLOL, (NDA) 019907
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
11/21/2006
025
Control Supplement
Letter
7/26/2002
018
Manufacturing Change or Addition
8/30/2001
017
Control Supplement
3/8/2001
016
Control Supplement
11/6/2000
015
Control Supplement
7/18/2000
014
Control Supplement
5/17/2000
013
Manufacturing Change or Addition
12/13/1999
012
Labeling Revision
12/13/1999
011
Control Supplement
5/19/1999
010
Control Supplement
5/20/1998
009
Control Supplement
10/21/1998
008
Manufacturing Change or Addition
3/21/1996
007
Labeling Revision
10/3/1997
006
Control Supplement
10/3/1997
005
Manufacturing Change or Addition
12/19/1996
004
Control Supplement
5/8/1995
003
Control Supplement
5/11/1995
002
Control Supplement
8/15/1994
001
Formulation Revision
12/29/1989
000
Approval
Therapeutic Equivalents
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