DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
AZASAN
FDA Application No:
(ANDA) 075252
Active Ingredient(s):
AZATHIOPRINE
Company:
AAIPHARMA LLC
Label History
Labels are not available on this site for AZASAN, (ANDA) 075252
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
2/3/2003
011
Labeling
2/3/2003
010
Facility Addition
2/3/2003
009
Chemistry New Strength
2/3/2003
008
Labeling
2/3/2003
007
Control Supplement
2/3/2003
006
Packaging Addition
2/3/2003
005
Chemistry New Strength
8/14/2002
004
Control Supplement
7/18/2001
003
Labeling
7/18/2001
002
Facility Addition
11/20/2000
001
Package Change
6/7/1999
000
Approval
Letter
Therapeutic Equivalents
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