Drugs@FDA: FDA-Approved Drugs

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New Drug Application (NDA): 050683
Company: PHARMACIA AND UPJOHN

Products on NDA 050683

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CONTAINER	CEFMETAZOLE SODIUM	EQ 20MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**	INJECTABLE;INJECTION	Discontinued	None	Yes	No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CONTAINER	CEFMETAZOLE SODIUM	EQ 40MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**	INJECTABLE;INJECTION	Discontinued	None	Yes	No

Approval Date(s) and History, Letters, Labels, Reviews for NDA 050683

Original Approvals or Tentative Approvals

Action Date	Submission	Action Type	Submission Classification	Review Priority; Orphan Status	Letters, Reviews, Labels, Patient Package Insert	Notes	Url
12/29/1992	ORIG-1	Approval	Type 3 - New Dosage Form	STANDARD		Label is not available on this site.