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ATOMOXETINE HYDROCHLORIDE

ANDA · Abbreviated New Drug Application (Generic) · Sponsor: ACTAVIS ELIZABETH · Approved 2012-05-11

Drug application

FDA Application #

ANDA078940

Application type

Abbreviated New Drug Application (Generic)

Brand name

ATOMOXETINE HYDROCHLORIDE

Generic name

Atomoxetine Hydrochloride

Active ingredients

ATOMOXETINE HYDROCHLORIDE

Dosage form

CAPSULE

Route

ORAL

Marketing status

None (Tentative Approval)

Sponsor

ACTAVIS ELIZABETH

First approval

2012-05-11

Source

Authoritative

Drugs@FDA application overview

Machine

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