TheraRadar
Data updated: Jul 17, 2026

BUPRENORPHINE HYDROCHLORIDE · Teva

CNS Approved 1981-12-29

Buprenorphine sublingual tablets is indicated for the treatment of opioid dependence and is preferred for induction. Buprenorphine sublingual tablets should be used as part of a complete treatment plan to include counseling and psychosocial support. Buprenorphine sublingual tablets should be used as part of a complete treatment plan that includes counseling and psychosocial support .

Source: FDA Label
15
Indications
--
Phase 3 Trials
44
Years on Market

Details

Status
Prescription
First Approved
1981-12-29
Routes
SUBLINGUAL, INJECTION
Dosage Forms
TABLET, INJECTABLE

BUPRENORPHINE HYDROCHLORIDE Approval History

1997
1998
1999
2000
2001
2002
2003
2004
2005
2006
2007
2008
2009
2010
2011
2012
2013
2014
2015
2016
2017
2018
2019
2020
2021
2022
2023
2024
2025
2026
Original
New Indication
New Form
Label Update
432 FDA actions from 1996 to 2026
Jul 2026 SUPPL
Mfg · Manufacturing (CMC)
Jan 2026 SUPPL
Label · Labeling
Dec 2025 SUPPL
Label · Labeling

What BUPRENORPHINE HYDROCHLORIDE Treats

1 indications

BUPRENORPHINE HYDROCHLORIDE is approved for 1 conditions since its original approval in 1996. These indications span multiple therapeutic areas including oncology, immunology, and more.

Same approved indications as BELBUCA (same active ingredient).

Source: FDA Label

Teva's other novel FDA approvals

Other CDER-designated drugs from the same sponsor (2016–2025).

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Active Pipeline

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Ongoing clinical trials by development phase

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Key Completed Trials

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Completed studies with published results, ranked by significance

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Trial Timeline

Full development history with FDA approval milestones

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Understanding FDA Approval Types
Count Type What it means
- ORIG Original approval - drug first enters market
- SUPPL - Efficacy New indication (new disease/condition approved)
- SUPPL - Labeling Label text changes (warnings, dosing updates)
- SUPPL - Manufacturing Production changes (new facility)
- SUPPL - Chemistry Formulation changes (new dosage strength)

Green lines in the timeline show ORIG and Efficacy approvals - the clinically meaningful milestones.

BUPRENORPHINE HYDROCHLORIDE FDA Label Details

Indications & Usage

Buprenorphine sublingual tablets is indicated for the treatment of opioid dependence and is preferred for induction. Buprenorphine sublingual tablets should be used as part of a complete treatment plan to include counseling and psychosocial support. Buprenorphine sublingual tablets contains buprenorphine, a partial opioid agonist, and is indicated for the treatment of opioid dependence and is preferred for induction. Buprenorphine sublingual tablets should be used as part of a complete treatment plan that includes counseling and psychosocial support .

Looking for the branded version?

BELBUCA

Full clinical data, patents, trials, and competitive landscape for buprenorphine hydrochloride.

See BELBUCA

Data Sources

Data sourced from official FDA and NIH databases. Click links to verify on original sources.