buprenorphine hydrochloride and naloxone hydrochloride

FDA Drug Profile — Zubsolv, Buprenorphine and Naloxone

Drug Details

Generic Name
buprenorphine hydrochloride and naloxone hydrochloride
Brand Names
Zubsolv, Buprenorphine and Naloxone
Application Number
NDA204242
Sponsor
Orexo US, Inc.
NDC Codes
8
Dosage Forms
TABLET, ORALLY DISINTEGRATING, TABLET
Routes
SUBLINGUAL
Active Ingredients
BUPRENORPHINE HYDROCHLORIDE, NALOXONE HYDROCHLORIDE

Indications and Usage

1 INDICATIONS AND USAGE Buprenorphine and Naloxone Sublingual Tablets are indicated for the maintenance treatment of opioid dependence. Buprenorphine and Naloxone Sublingual Tablets should be used as part of a complete treatment plan to include counseling and psychosocial support. Buprenorphine and Naloxone Sublingual Tablets contain buprenorphine, a partial opioid agonist, and naloxone, an opioid antagonist, and are indicated for the maintenance treatment of opioid dependence. ( ) Buprenorphine and Naloxone Sublingual Tablets should be used as part of a complete treatment plan that includes counseling and psychosocial support. ( )