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ORUDIS

NDA · New Drug Application · Sponsor: WYETH AYERST · Approved 1986-01-09

Drug application

FDA Application #

NDA018754

Application type

New Drug Application

Brand name

ORUDIS

Generic name

Ketoprofen

Active ingredients

KETOPROFEN

Dosage form

CAPSULE

Route

ORAL

Marketing status

Discontinued

Sponsor

WYETH AYERST

First approval

1986-01-09

Source

Authoritative

Drugs@FDA application overview

Machine

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