DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
METHOTREXATE SODIUM
FDA Application No:
(ANDA) 081099
Active Ingredient(s):
METHOTREXATE SODIUM
Company:
BARR
Label History
Labels are not available on this site for METHOTREXATE SODIUM, (ANDA) 081099
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
8/22/2002
027
Labeling
8/22/2002
026
Labeling
8/10/2000
025
Labeling
12/20/2000
024
Supplier Addition
12/21/1999
023
Facility Addition
12/6/1999
022
Facility Addition
7/6/1999
021
Chemistry
7/6/1999
020
Labeling
7/6/1999
019
Chemistry
5/20/1999
018
Chemistry
11/20/1998
017
Chemistry
11/20/1998
016
Chemistry
11/20/1998
015
Chemistry
12/1/1998
014
Chemistry
8/17/1998
013
Chemistry
6/9/1998
012
Labeling
10/30/1997
011
Chemistry
4/3/1996
010
Chemistry
4/18/1996
009
Chemistry
12/23/1994
008
Chemistry
4/3/1992
007
Chemistry
4/3/1992
005
Chemistry
9/26/1994
004
Labeling
9/26/1994
003
Chemistry
12/19/1991
002
Labeling
5/10/1991
001
Chemistry Expedite
10/15/1990
000
Approval
Therapeutic Equivalents
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