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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 207667
Company: EUGIA PHARMA
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
METHYLPREDNISOLONE SODIUM SUCCINATE METHYLPREDNISOLONE SODIUM SUCCINATE EQ 40MG BASE/VIAL INJECTABLE;INJECTION Discontinued None No No
METHYLPREDNISOLONE SODIUM SUCCINATE METHYLPREDNISOLONE SODIUM SUCCINATE EQ 125MG BASE/VIAL INJECTABLE;INJECTION Discontinued None No No
METHYLPREDNISOLONE SODIUM SUCCINATE METHYLPREDNISOLONE SODIUM SUCCINATE EQ 500MG BASE/VIAL INJECTABLE;INJECTION Discontinued None No No
METHYLPREDNISOLONE SODIUM SUCCINATE METHYLPREDNISOLONE SODIUM SUCCINATE EQ 2GM BASE/VIAL INJECTABLE;INJECTION 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
12/15/2015 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
04/02/2020 SUPPL-2 Labeling-Package Insert

Label is not available on this site.

04/02/2020 SUPPL-1 Labeling-Package Insert

Label is not available on this site.

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