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Drugs@FDA: FDA-Approved Drugs

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New Drug Application:
Company:
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
Original Approvals or Tentative Approvals
Action Date Submission Action Type Submission Classification Review Priority; Orphan Status Letters, Reviews, Labels, Patient Package Insert Notes Url
01/08/2010 ORIG-1 Approval

Label is not available on this site.

Supplements
Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels, Patient Package Insert Note Url
02/24/2017 SUPPL-6 Labeling-Package Insert

Label is not available on this site.

03/30/2012 SUPPL-1 Labeling-Package Insert

Label is not available on this site.

METHOTREXATE SODIUM PRESERVATIVE FREE

INJECTABLE;INJECTION; EQ 250MG/10ML (EQ 25MG BASE/ML)
TE Code = AP

Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status RLD TE Code Application No. Company
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