TheraRadar
Data updated: May 26, 2026

FORFIVO XL (bupropion hydrochloride)

Trial Activity: Declining
CNS Approved 2011-11-10

FORFIVO XL is indicated for the treatment of Major Depressive Disorder.

Source: FDA Label • TWI PHARMS

How FORFIVO XL Works

The exact mechanism of action for bupropion is unknown, though its therapeutic effects are presumed to be mediated by noradrenergic and dopaminergic mechanisms. The drug acts as a relatively weak inhibitor of the neuronal uptake of norepinephrine and dopamine. Unlike some other classes of antidepressants, it does not inhibit monoamine oxidase or the reuptake of serotonin.

Development Insights

Pfizer conducting 2 trials (40%)
9 indications explored (Moderate)
smoking cessation (3 trials)
wilson disease (1 trials)
smoking, tobacco (1 trials)
1
Indication
--
Phase 3 Trials
14
Years on Market

Details

Status
Prescription
First Approved
2011-11-10
Patent Cliff
2028

Pro Metrics

Patent cliff and revenue data

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Routes
ORAL
Dosage Forms
TABLET, EXTENDED RELEASE

Companies

Active Ingredient: BUPROPION HYDROCHLORIDE

FORFIVO XL Approval History

2012
2013
2014
2015
2016
2017
2018
2019
2020
2021
2022
2023
2024
2025
2026
Original
New Indication
New Form
Label Update
7 FDA actions from 2011 to 2025
Nov 2025 SUPPL
Label · Labeling
May 2024 SUPPL
Label · Labeling
Dec 2019 SUPPL
Label · Labeling

What FORFIVO XL Treats

1 indications

FORFIVO XL is approved for 1 conditions since its original approval in 2011. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Major Depressive Disorder
Source: FDA Label

FORFIVO XL Boxed Warning

SUICIDAL THOUGHTS AND BEHAVIORS SUICIDALITY AND ANTIDEPRESSANT DRUGS Antidepressants increased the risk of suicidal thoughts and behavior in children, adolescents, and young adults in short‑term trials. These trials did not show an increase in the risk of suicidal thoughts and behavior with antidepressant use in subjects over age 24; there was a reduction in risk with antidepressant use in subjects aged 65 and older [see Warnings and Precautions (5.1)] . In patients of all ages who are started o...

FORFIVO XL Competitive Set

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Three rings of competition based on shared molecular targets and treated indications.

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Filters applied: drops same-active-ingredient (505(b)(2) reformulations), route-mismatch (topical vs systemic), and cross-therapeutic-area matches in same-indication rings.

Drugs Similar to FORFIVO XL

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Clinical Trial Registry

5 trials
Trial Sponsor ID Phase Status Title
NCT04526210 results posted ALXN1840-HV-103 Ph 1 completed Study of ALXN1840 on the Metabolism of a CYP2B6 Substrate in Healthy Participants
NCT03326128 1703346 Ph 2 terminated High Dose Bupropion for Smoking Cessation - Pilot Study
NCT01574703 CATS results posted A3051148 2011-005513-37, CATS Ph 4 completed Study To Evaluate Cardiac Assessments Following Different Treatments Of Smoking Cessation Medications In Subjects With And Without Psychiatric Disorders.
NCT01456936 EAGLES results posted A3051123 2010-022914-15, EAGLES Ph 4 completed Study Evaluating The Safety And Efficacy Of Varenicline and Bupropion For Smoking Cessation In Subjects With And Without A History Of Psychiatric Disorders
NCT01635972 9766-CL-0044 Ph 1 completed Drug Interaction Study of Multiple Doses of Isavuconazole and a Single Dose of Bupropion
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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.

FORFIVO XL FDA Label Details

Indications & Usage

FDA Label (PDF)

FORFIVO XL is indicated for the treatment of Major Depressive Disorder.

⚠️ BOXED WARNING

WARNING: SUICIDAL THOUGHTS AND BEHAVIORS SUICIDALITY AND ANTIDEPRESSANT DRUGS Antidepressants increased the risk of suicidal thoughts and behavior in children, adolescents, and young adults in short‑term trials. These trials did not show an increase in the risk of suicidal thoughts and behavior with...

View full patent landscape →
1 OB patents · 1 families · 2 international docs across 1 countries

FORFIVO XL Patents & Exclusivity

Latest Patent: Aug 2028

Patents (1 active)

US7674479 Expires Aug 23, 2028
Source: FDA Orange Book

Pro Intelligence Preview

Deep insights for FORFIVO XL

Revenue Insights

  • Quarterly revenue tracking
  • Historical trend analysis

Patent Timeline

  • Cliff: 2028
  • 1 active patents

Trial Analysis

  • 5 total trials
  • Stage: Declining

Competitive Landscape

  • 20 similar drugs
  • Same target/indication analysis
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Full approval history • All patents • Revenue trends • Competitor analysis

Data Sources

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

How We Calculate These Metrics

Trial Activity Stage

Measures the current development activity pattern based on trial phases, status, and trends. Important: This measures R&D activity, not commercial lifecycle.

Trial statuses: "Active" means recruiting or ongoing. "Completed" means reached planned endpoint. "Terminated" means stopped early—often due to safety, efficacy, or business reasons.

  • Growth: High proportion of early-phase trials (Phase 1/2), active development
  • Expansion: Significant Phase 3 activity, approaching or pursuing approvals
  • Mature: Substantial Phase 4 post-marketing studies
  • Stable: Mixed phase distribution, steady development
  • Declining: Low active trial ratio, reduced R&D investment