Composition
- Active ingredients
- BUPRENORPHINE HYDROCHLORIDE EQ 4.2MG BASE; NALOXONE HYDROCHLORIDE EQ 0.7MG BASE
Strengths and forms
The FDA lists each strength of a product separately; these pages share one label.
- BUPRENORPHINE HYDROCHLORIDE EQ 4.2MG BASE; NALOXONE HYDROCHLORIDE EQ 0.7MG BASE · FilmThis page
- BUPRENORPHINE HYDROCHLORIDE EQ 6.3MG BASE; NALOXONE HYDROCHLORIDE EQ 1MG BASE · FilmNDA205637-003 · Discontinued
- BUPRENORPHINE HYDROCHLORIDE EQ 2.1MG BASE; NALOXONE HYDROCHLORIDE EQ 0.3MG BASE · FilmNDA205637-001 · Discontinued
Official product information
Drugs@FDA lists the approved labels, letters and reviews for application NDA205637.
Prognia shows this product information for reference and learning. It is not treatment advice and can lag behind the official text. Always check the current product information and local protocols before prescribing.
At a glance
- Brand name
- Bunavail
- Active substance
- buprenorphine hydrochloride
- Route
- Buccal
- Dosage form
- Film
- Applicant
- Bdsi
- Status
- Discontinued
- FDA approval
- 6 Jun 2014
- Application
- NDA205637-002