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METHYLDOPA AND HYDROCHLOROTHIAZIDE

ANDA · Abbreviated New Drug Application (Generic) · Sponsor: WATSON LABS · Approved 1989-02-06

Drug application

FDA Application #

ANDA070958

Application type

Abbreviated New Drug Application (Generic)

Brand name

METHYLDOPA AND HYDROCHLOROTHIAZIDE

Generic name

Hydrochlorothiazide

Active ingredients

HYDROCHLOROTHIAZIDE; METHYLDOPA

Dosage form

TABLET

Route

ORAL

Marketing status

Discontinued

Sponsor

WATSON LABS

First approval

1989-02-06

Source

Authoritative

Drugs@FDA application overview

Machine

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