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) 072619
Active Ingredient(s):
ALBUTEROL SULFATE
Company:
TEVA
Label History
Labels are not available on this site for ALBUTEROL SULFATE, (ANDA) 072619
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
6/12/1998
015
Labeling
6/18/1997
014
Chemistry
12/23/1994
013
Chemistry
2/16/1995
012
Chemistry
9/6/1994
011
Chemistry
6/17/1994
010
Chemistry
4/21/1994
009
Chemistry in Effect
4/21/1994
008
Chemistry in Effect
11/15/1993
007
Chemistry in Effect
3/1/1993
006
Labeling in Effect
11/5/1992
004
Labeling in Effect
3/6/1992
003
Chemistry in Effect
6/18/1991
002
Labeling
1/17/1991
001
Labeling
4/7/1989
000
Approval
Therapeutic Equivalents
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