APPLICATION
ANDA065002
TYPE
ANDA
ORIGINAL APPROVAL
1998-09-28
LATEST ACTION
2009-09-29
ROUTE
INJECTION
DOSAGE FORM
INJECTABLE
MARKETING STATUS
Discontinued
Products
CEFUROXIME SODIUMDiscontinued
CEFUROXIME SODIUM EQ 7.5GM BASE/VIAL · INJECTABLE · INJECTION
Approval history
2009-09-29Labeling · Supplement 7AP
2008-03-31Labeling · Supplement 6AP
2004-02-20Labeling · Supplement 4AP
2003-04-30Labeling · Supplement 3AP
2002-10-10Labeling · Supplement 2AP
2002-03-28Manufacturing (CMC) · Supplement 1AP
Source: FDA Drugs@FDA. SPEQ is not affiliated with the FDA; this is a reference view of public FDA data, not medical, legal, or regulatory advice.
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