DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
MEXATE-AQ PRESERVED
FDA Application No:
(ANDA) 089887
Active Ingredient(s):
METHOTREXATE SODIUM
Company:
BRISTOL MYERS SQUIBB
Label History
Labels are not available on this site for MEXATEAQ PRESERVED, (ANDA) 089887
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
7/30/1990
001
Labeling
4/14/1989
000
Approval
Therapeutic Equivalents
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