DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
ACETAMINOPHEN AND HYDROCODONE BITARTRATE
FDA Application No:
(ANDA) 088898
Active Ingredient(s):
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Company:
CENT PHARMS
Label History
Labels are not available on this site for ACETAMINOPHEN AND HYDROCODONE BITARTRATE, (ANDA) 088898
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
11/29/1999
018
Facility Addition
9/12/1996
017
Chemistry
12/20/1994
016
Chemistry
1/24/1994
015
Chemistry
1/24/1994
014
Chemistry
1/24/1994
013
Chemistry
1/24/1994
012
Labeling
1/24/1994
011
Chemistry
11/29/1989
009
Labeling
1/8/1993
007
Chemistry
10/19/1992
006
Chemistry
11/21/1989
005
Labeling
10/19/1992
004
Labeling
3/27/1985
000
Approval
There are no Therapeutic Equivalents
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