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PROZAC WEEKLY

NDA · New Drug Application · Sponsor: LILLY · Approved 2001-02-26

Drug application

FDA Application #

NDA021235

Application type

New Drug Application

Brand name

PROZAC WEEKLY

Generic name

Fluoxetine Hydrochloride

Active ingredients

FLUOXETINE HYDROCHLORIDE

Dosage form

CAPSULE, DELAYED REL PELLETS

Route

ORAL

Marketing status

Discontinued

Sponsor

LILLY

First approval

2001-02-26

Source

Authoritative

Drugs@FDA application overview

Machine

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