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ISMELIN

NDA · New Drug Application · Sponsor: NOVARTIS · Approved 1960-07-05

Drug application

FDA Application #

NDA012329

Application type

New Drug Application

Brand name

ISMELIN

Generic name

Guanethidine Monosulfate

Active ingredients

GUANETHIDINE MONOSULFATE

Dosage form

TABLET

Route

ORAL

Marketing status

Discontinued

Sponsor

NOVARTIS

First approval

1960-07-05

Source

Authoritative

Drugs@FDA application overview

Machine

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