APPLICATION
NDA050581
TYPE
NDA
LATEST ACTION
1997-02-27
ROUTE
INJECTION
DOSAGE FORM
INJECTABLE
MARKETING STATUS
Discontinued
Products
MEFOXIN IN DEXTROSE 5% IN PLASTIC CONTAINER · ReferenceDiscontinued
CEFOXITIN SODIUM EQ 40MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · INJECTABLE · INJECTION
MEFOXIN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER · ReferenceDiscontinued
CEFOXITIN SODIUM EQ 20MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · INJECTABLE · INJECTION
MEFOXIN IN DEXTROSE 5% IN PLASTIC CONTAINER · ReferenceDiscontinued
CEFOXITIN SODIUM EQ 20MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · INJECTABLE · INJECTION
MEFOXIN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER · ReferenceDiscontinued
CEFOXITIN SODIUM EQ 40MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · INJECTABLE · INJECTION
Approval history
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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