DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
ACETAMINOPHEN AND CODEINE PHOSPHATE
FDA Application No:
(NDA) 040223
Active Ingredient(s):
ACETAMINOPHEN; CODEINE PHOSPHATE
Company:
DURAMED PHARMS BARR
Label History
Labels are not available on this site for ACETAMINOPHEN AND CODEINE PHOSPHATE, (NDA) 040223
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
12/9/2002
014
Control Supplement
12/9/2002
013
Manufacturing Revision
12/9/2002
012
Facility Addition
4/9/2002
011
Facility Addition
4/9/2002
010
Facility Addition
4/9/2002
009
Package Change
4/9/2002
008
Facility Addition
6/5/2000
007
Supplier Addition
6/5/2000
006
Formulation Revision
6/5/2000
005
Labeling
6/5/2000
004
Control Supplement
6/5/2000
003
Package Change
6/5/2000
002
Manufacturing Revision
5/20/1999
001
Control Supplement
11/18/1997
000
Approval
There are no Therapeutic Equivalents
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