# BUNAVAIL
> **NDA205637** · New Drug Application · Sponsor: BDSI · Approved 2014-06-06
## Drug
- **FDA Application Number:** 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
- [Drugs@FDA application overview](https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=205637)
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