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) 074454
Active Ingredient(s):
ALBUTEROL SULFATE
Company:
ACTAVIS MID ATLANTIC
Label History
Labels are not available on this site for ALBUTEROL SULFATE, (ANDA) 074454
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
12/3/2002
011
Control Supplement
5/18/2001
010
Package Change
10/16/2000
008
Package Change
7/13/1999
006
Labeling
7/7/1999
005
Chemistry
7/7/1999
004
Labeling
7/7/1999
003
Chemistry
1/12/1999
002
Labeling
9/25/1995
000
Approval
Therapeutic Equivalents
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