DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
ACETYLCYSTEINE
FDA Application No:
(ANDA) 072323
Active Ingredient(s):
ACETYLCYSTEINE
Company:
BEDFORD
Label History
Labels are not available on this site for ACETYLCYSTEINE, (ANDA) 072323
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
4/3/2001
005
Microbiology
12/4/2000
004
Control Supplement
6/18/1996
003
Chemistry
5/23/1995
002
Chemistry
4/30/1992
000
Approval
Therapeutic Equivalents
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