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Abbreviated New Drug Application (ANDA): 064170
Company: FRESENIUS KABI USA
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
CEFAZOLIN SODIUM CEFAZOLIN SODIUM EQ 10GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** INJECTABLE;INJECTION Discontinued None No No
CEFAZOLIN SODIUM CEFAZOLIN SODIUM EQ 20GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** INJECTABLE;INJECTION Discontinued None No No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
03/18/1998 ORIG-1 Approval Review

Label is not available on this site.

https://www.accessdata.fda.gov/drugsatfda_docs/anda/98/64170.cfm
Supplements
Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels, Patient Package Insert Note Url
05/29/2009 SUPPL-13 Labeling

Label is not available on this site.

01/27/2006 SUPPL-11 Labeling

Label is not available on this site.

04/20/2005 SUPPL-7 Labeling

Label is not available on this site.

03/08/2004 SUPPL-6 Labeling

Label is not available on this site.

08/15/2003 SUPPL-4 Labeling

Label is not available on this site.

05/08/2002 SUPPL-3 Manufacturing (CMC)-Control

Label is not available on this site.

05/07/2001 SUPPL-2 Manufacturing (CMC)

Label is not available on this site.

05/07/2001 SUPPL-1 Manufacturing (CMC)-Control

Label is not available on this site.

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