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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 211272
Company: TEVA PHARMS USA
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
MYCOPHENOLATE MOFETIL MYCOPHENOLATE MOFETIL 200MG/ML FOR SUSPENSION;ORAL Discontinued None No No
Original Approvals or Tentative Approvals
Action Date Submission Action Type Submission Classification Review Priority; Orphan Status Letters, Reviews, Labels, Patient Package Insert Notes Url
01/25/2022 ORIG-1 Approval STANDARD

Label is not available on this site.

Supplements
Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels, Patient Package Insert Note Url
08/13/2024 SUPPL-3 REMS - MODIFIED - D-N-A

Label is not available on this site.

10/17/2024 SUPPL-2 Labeling-Package Insert, Labeling-Medication Guide

Label is not available on this site.

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