DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
ALBUTEROL SULFATE
FDA Application No:
(ANDA) 072152
Active Ingredient(s):
ALBUTEROL SULFATE
Company:
SANDOZ
Label History
Labels are not available on this site for ALBUTEROL SULFATE, (ANDA) 072152
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
4/19/2002
017
Control Supplement
12/13/2001
016
Control Supplement
2/7/2002
015
Control Supplement
11/30/2000
014
Control Supplement
4/23/1998
013
Labeling
11/5/1997
012
Chemistry
12/7/1995
011
Chemistry
8/23/1994
010
Labeling
1/24/1994
009
Chemistry
8/23/1994
007
Chemistry
8/23/1994
006
Chemistry
8/23/1994
005
Chemistry
10/6/1993
004
Labeling
7/10/1991
003
Labeling in Effect
9/10/1990
002
Labeling in Effect
10/18/1989
001
Labeling in Effect
3/23/1989
000
Approval
Therapeutic Equivalents
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