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FDA ANDA · ANDA064124

CEFUROXIME SODIUM

Sponsor: ACS DOBFAR SPA

APPLICATION
ANDA064124
TYPE
ANDA
ORIGINAL APPROVAL
1997-05-30
LATEST ACTION
2021-10-08
ROUTE
INJECTION
DOSAGE FORM
INJECTABLE
MARKETING STATUS
Discontinued

Products

CEFUROXIME SODIUMDiscontinued
CEFUROXIME SODIUM EQ 7.5GM BASE/VIAL · INJECTABLE · INJECTION

Approval history

2021-10-08Labeling · Supplement 18 · standardAP
2008-07-31Labeling · Supplement 8AP
2007-11-16Labeling · Supplement 7AP
2007-06-20Labeling · Supplement 6AP
2007-01-31Labeling · Supplement 5AP
2004-09-30Labeling · Supplement 3AP
1999-09-23Manufacturing (CMC) · Supplement 1AP
1997-05-30OriginalAP
VIEW ON DRUGS@FDA ↗

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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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