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OCUPRESS

NDA · New Drug Application · Sponsor: NOVARTIS · Approved 1990-05-23

Drug application

FDA Application #

NDA019972

Application type

New Drug Application

Brand name

OCUPRESS

Generic name

Carteolol Hydrochloride

Active ingredients

CARTEOLOL HYDROCHLORIDE

Dosage form

SOLUTION/DROPS

Route

OPHTHALMIC

Marketing status

Discontinued

Sponsor

NOVARTIS

First approval

1990-05-23

Source

Authoritative

Drugs@FDA application overview

Machine

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