DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
TALWIN COMPOUND
FDA Application No:
(NDA) 016891
Active Ingredient(s):
ASPIRIN; PENTAZOCINE HYDROCHLORIDE
Company:
SANOFI AVENTIS US
Label History
Labels are not available on this site for TALWIN COMPOUND, (NDA) 016891
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
11/29/1995
020
Control Supplement
7/25/1996
019
Control Supplement
1/3/1991
018
Labeling Revision
3/17/1988
017
Manufacturing Change or Addition
1/5/1989
016
Labeling Revision
1/5/1989
015
Labeling Revision
3/9/1982
014
Expiration Date Change
12/1/1981
013
Package Change
10/2/1981
011
Labeling Revision
11/5/1980
010
Expiration Date Change
1/5/1989
009
Labeling Revision
5/30/1979
008
Manufacturing Change or Addition
5/8/1979
007
Package Change
5/8/1979
006
Package Change
12/9/1977
004
Package Change
5/8/1979
003
Control Supplement
5/13/1977
002
Labeling Revision
2/23/1976
001
Manufacturing Change or Addition
11/12/1975
000
Approval
There are no Therapeutic Equivalents
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