DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
THEOCHRON
FDA Application No:
(ANDA) 088320
Active Ingredient(s):
THEOPHYLLINE
Company:
INWOOD LABS
Label History
Labels are not available on this site for THEOCHRON, (ANDA) 088320
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
10/11/2002
022
Package Change
1/28/1998
021
Chemistry
2/7/1997
020
Labeling
7/7/1997
019
Chemistry
7/7/1997
018
Chemistry
10/17/1996
017
Labeling
1/23/1996
016
Labeling
2/22/1993
015
Chemistry
4/2/1990
014
Labeling
10/6/1989
013
Labeling
1/25/1989
012
SBA
3/24/1989
012
Labeling
6/20/1988
011
Chemistry
2/9/1988
007
Chemistry
2/9/1988
006
Chemistry
2/9/1988
005
Chemistry
4/29/1986
003
Chemistry
5/11/1987
002
Chemistry
9/19/1985
001
Chemistry
2/21/1985
000
Approval
Therapeutic Equivalents
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