DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
PROVENTIL
FDA Application No:
(NDA) 019383
Active Ingredient(s):
ALBUTEROL SULFATE
Company:
SCHERING
Label History
Labels are not available on this site for PROVENTIL, (NDA) 019383
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
4/9/2001
019
Control Supplement
7/15/1998
013
Manufacturing Change or Addition
9/18/1997
011
New or Modified Indication
11/6/1998
010
Labeling Revision
Review
5/24/1999
009
Control Supplement
9/9/1996
008
Manufacturing Change or Addition
5/27/1993
004
Control Supplement
12/12/1997
003
Control Supplement
6/5/1992
002
Control Supplement
1/24/1989
001
Manufacturing Change or Addition
7/13/1987
000
Approval
Therapeutic Equivalents
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