Drugs@FDA: FDA-Approved Drugs

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New Drug Application (NDA): 018754
Company: WYETH AYERST

Products on NDA 18754

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	TE Code	RLD	RS
ORUDIS	KETOPROFEN	25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**	CAPSULE;ORAL	Discontinued	None	Yes	No
ORUDIS	KETOPROFEN	50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**	CAPSULE;ORAL	Discontinued	None	Yes	No
ORUDIS	KETOPROFEN	75MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**	CAPSULE;ORAL	Discontinued	None	Yes	No