Drugs@FDA: FDA-Approved Drugs

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New Drug Application (NDA): 050581
Company: MERCK

Products on NDA 050581

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	TE Code	RLD	RS
MEFOXIN IN DEXTROSE 5% IN PLASTIC CONTAINER	CEFOXITIN SODIUM	EQ 20MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**	INJECTABLE;INJECTION	Discontinued	None	Yes	No
MEFOXIN IN DEXTROSE 5% IN PLASTIC CONTAINER	CEFOXITIN SODIUM	EQ 40MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**	INJECTABLE;INJECTION	Discontinued	None	Yes	No
MEFOXIN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER	CEFOXITIN SODIUM	EQ 40MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**	INJECTABLE;INJECTION	Discontinued	None	Yes	No
MEFOXIN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER	CEFOXITIN SODIUM	EQ 20MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**	INJECTABLE;INJECTION	Discontinued	None	Yes	No

Approval Date(s) and History, Letters, Labels, Reviews for NDA 050581

Supplements

Action Date	Submission	Supplement Categories or Approval Type	Letters, Reviews, Labels, Patient Package Insert	Note	Url
02/27/1997	SUPPL-20		Review	Label is not available on this site.	https://www.accessdata.fda.gov/drugsatfda_docs/nda/97/50-517s031_50-581s020_Mefoxin.html