APPLICATION
NDA050683
TYPE
NDA
ORIGINAL APPROVAL
1992-12-29
LATEST ACTION
1992-12-29
ROUTE
INJECTION
DOSAGE FORM
INJECTABLE
MARKETING STATUS
Discontinued
Products
ZEFAZONE IN PLASTIC CONTAINER · ReferenceDiscontinued
CEFMETAZOLE SODIUM EQ 20MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · INJECTABLE · INJECTION
ZEFAZONE IN PLASTIC CONTAINER · ReferenceDiscontinued
CEFMETAZOLE SODIUM EQ 40MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · INJECTABLE · INJECTION
Approval history
1992-12-29Type 3 - New Dosage Form · Original · standardAP
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.
Weekly Briefing
Read a past issue →Get the Weekly GxP Briefing
Curated regulatory intelligence — enforcement, recalls, guidance, and quality signals — in one practitioner-grade email each week. Free.