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) 072779
Active Ingredient(s):
ALBUTEROL SULFATE
Company:
TEVA
Label History
Labels are not available on this site for ALBUTEROL SULFATE, (ANDA) 072779
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
10/20/1998
004
Chemistry
5/14/1998
003
Labeling
2/4/1994
002
Chemistry
7/15/1993
001
Labeling in Effect
6/25/1993
000
Approval
Therapeutic Equivalents
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