Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 065232
Company: HOSPIRA INC
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
CEFTRIAXONE CEFTRIAXONE SODIUM EQ 10GM 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
08/02/2005 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
02/17/2012 SUPPL-13 Labeling-Package Insert

Label is not available on this site.

09/10/2010 SUPPL-12 Labeling-Package Insert

Label is not available on this site.

08/27/2009 SUPPL-11 Labeling

Label is not available on this site.

08/27/2009 SUPPL-10 Labeling

Label is not available on this site.

11/14/2008 SUPPL-9 Labeling

Label is not available on this site.

11/14/2008 SUPPL-6 Labeling

Label is not available on this site.

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