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UNIRETIC

NDA · New Drug Application · Sponsor: UCB INC · Approved 1997-06-27

Drug application

FDA Application #

NDA020729

Application type

New Drug Application

Brand name

UNIRETIC

Generic name

Hydrochlorothiazide

Active ingredients

HYDROCHLOROTHIAZIDE; MOEXIPRIL HYDROCHLORIDE

Dosage form

TABLET

Route

ORAL

Marketing status

Discontinued

Sponsor

UCB INC

First approval

1997-06-27

Source

Authoritative

Drugs@FDA application overview

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