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BUNAVAIL

NDA · New Drug Application · Sponsor: BDSI · Approved 2014-06-06

Drug application

FDA Application #

NDA205637

Application type

New Drug Application

Brand name

BUNAVAIL

Generic name

Buprenorphine Hydrochloride

Active ingredients

BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE

Dosage form

FILM

Route

BUCCAL

Marketing status

Discontinued

Sponsor

BDSI

First approval

2014-06-06

Source

Authoritative

Drugs@FDA application overview

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