DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
ACETAMINOPHEN
FDA Application No:
(ANDA) 076200
Active Ingredient(s):
ACETAMINOPHEN
Company:
COREPHARMA
Label History
Labels are not available on this site for ACETAMINOPHEN, (ANDA) 076200
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
8/11/2004
005
Supplement
Review
12/3/2002
004
Package Change
Review
12/3/2002
003
Packager Addition
Review
12/3/2002
002
Packager Addition
Review
10/15/2002
001
Control Supplement
Review
3/19/2002
000
Approval
Letter
Review
Therapeutic Equivalents
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