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) 072637
Active Ingredient(s):
ALBUTEROL SULFATE
Company:
MUTUAL PHARM
Label History
Labels are not available on this site for ALBUTEROL SULFATE, (ANDA) 072637
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
12/11/2002
017
Control Supplement
7/3/2002
016
Control Supplement
3/4/2002
015
Control Supplement
5/1/2002
014
Control Supplement
5/16/2000
013
Facility Addition
5/16/2000
012
Facility Addition
6/12/1998
011
Labeling
12/5/1997
010
Chemistry
2/24/1997
009
Chemistry
6/22/1995
008
Chemistry
1/12/1994
007
Chemistry
10/25/1993
006
Chemistry
2/9/1993
005
Labeling
11/5/1992
004
Labeling
2/4/1991
003
Labeling
8/29/1990
002
Labeling
3/22/1989
001
Labeling
2/1/1989
000
Approval
Therapeutic Equivalents
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