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DUEXIS

NDA · New Drug Application · Sponsor: HORIZON · Approved 2011-04-23

Drug application

FDA Application #

NDA022519

Application type

New Drug Application

Brand name

DUEXIS

Generic name

Famotidine

Active ingredients

FAMOTIDINE; IBUPROFEN

Dosage form

TABLET

Route

ORAL

Marketing status

Discontinued

Sponsor

HORIZON

First approval

2011-04-23

Source

Authoritative

Drugs@FDA application overview

Machine

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