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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 065313
Company: HOSPIRA INC
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
CEFOXITIN CEFOXITIN SODIUM EQ 1GM BASE/VIAL INJECTABLE;INJECTION Discontinued None No No
CEFOXITIN CEFOXITIN 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
01/23/2006 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
04/22/2014 SUPPL-10 Labeling-Package Insert

Label is not available on this site.

03/05/2008 SUPPL-5 Labeling

Label is not available on this site.

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