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FDA ANDA · ANDA065071

CEFOTAXIME

Sponsor: HIKMA

APPLICATION
ANDA065071
TYPE
ANDA
ORIGINAL APPROVAL
2002-11-20
LATEST ACTION
2020-06-08
ROUTE
INTRAVENOUS, INJECTION
DOSAGE FORM
INJECTABLE
MARKETING STATUS
Discontinued

Products

CEFOTAXIMEDiscontinued
CEFOTAXIME SODIUM EQ 10GM BASE/VIAL · INJECTABLE · INJECTION

Approval history

2020-06-08Labeling · Supplement 14 · standardAP
2020-06-08Labeling · Supplement 12 · standardAP
2020-06-08Labeling · Supplement 11 · standardAP
2002-11-20OriginalAP
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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