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) 075394
Active Ingredient(s):
ALBUTEROL SULFATE
Company:
MORTON GROVE
Label History
Labels are not available on this site for ALBUTEROL SULFATE, (ANDA) 075394
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
10/15/2001
004
Control Supplement
5/30/2001
003
Packaging Addition
5/30/2001
002
Packaging Addition
5/30/2001
001
Labeling
11/22/1999
000
Approval
Letter
Review
Therapeutic Equivalents
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