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) 072859
Active Ingredient(s):
ALBUTEROL SULFATE
Company:
CLONMEL HLTHCARE
Label History
Labels are not available on this site for ALBUTEROL SULFATE, (ANDA) 072859
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
12/13/1993
005
Labeling in Effect
12/30/1993
004
Chemistry in Effect
7/22/1993
003
Labeling
11/23/1990
002
Labeling
8/31/1990
001
Labeling
12/20/1989
000
Approval
Therapeutic Equivalents
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