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LERITINE

NDA · New Drug Application · Sponsor: MERCK · Approved 1957-08-15

Drug application

FDA Application #

NDA010585

Application type

New Drug Application

Brand name

LERITINE

Generic name

Anileridine Hydrochloride

Active ingredients

ANILERIDINE HYDROCHLORIDE

Dosage form

TABLET

Route

ORAL

Marketing status

Discontinued

Sponsor

MERCK

First approval

1957-08-15

Source

Authoritative

Drugs@FDA application overview

Machine

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