Visitor Monitoring Drug History: METHOTREXATE SODIUM
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
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Label and Approval History

Drug Name: METHOTREXATE SODIUM
FDA Application No: (NDA) 040263
Active Ingredient(s): METHOTREXATE SODIUM
Company: ABRAXIS PHARM
 
Label History
 
View the label approved on June 9, 2004 for METHOTREXATE SODIUM, (NDA) 040263


To see older, previously-approved labels, go to the "Approval History" section of this page. Older labels are for historical information only and should not be used for clinical purposes.
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
12/2/2002 001Control Supplement  
2/26/1999 000Approval Letter
Label
Review 
 
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