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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 065124
Company: LUPIN
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
CEFOTAXIME SODIUM CEFOTAXIME SODIUM EQ 500MG BASE/VIAL INJECTABLE;INJECTION Discontinued None No No
CEFOTAXIME SODIUM CEFOTAXIME SODIUM EQ 1GM BASE/VIAL INJECTABLE;INJECTION Discontinued None No No
CEFOTAXIME SODIUM CEFOTAXIME SODIUM 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
09/24/2003 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
03/11/2013 SUPPL-9 Labeling-Package Insert

Label is not available on this site.

09/30/2011 SUPPL-4 Labeling-Package Insert

Label is not available on this site.

06/09/2005 SUPPL-1 Labeling

Label is not available on this site.

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