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FDA ANDA · ANDA075843

OXAPROZIN

Sponsor: ACTAVIS ELIZABETH

APPLICATION
ANDA075843
TYPE
ANDA
ORIGINAL APPROVAL
2001-10-03
LATEST ACTION
2003-04-18
ROUTE
ORAL
DOSAGE FORM
TABLET
MARKETING STATUS
Discontinued

Products

OXAPROZINDiscontinued
OXAPROZIN 600MG · TABLET · ORAL

Approval history

2003-04-18Labeling · Supplement 3AP
2002-03-13Manufacturing (CMC) · Supplement 1AP
2001-10-03OriginalLetterAP
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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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