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Bupropion

Generic Name
Bupropion
Brand Names
Aplenzin, Auvelity, Budeprion, Contrave, Forfivo, Wellbutrin, Zyban, Mysimba
Drug Type
Small Molecule
Chemical Formula
C13H18ClNO
CAS Number
34911-55-2
Unique Ingredient Identifier
01ZG3TPX31

Overview

Bupropion (also known as the brand name product Wellbutrin®) is a norepinephrine/dopamine-reuptake inhibitor (NDRI) used most commonly for the management of Major Depressive Disorder (MDD), Seasonal Affective Disorder (SAD), and as an aid for smoking cessation. Bupropion exerts its pharmacological effects by weakly inhibiting the enzymes involved in the uptake of the neurotransmitters norepinephrine and dopamine from the synaptic cleft, therefore prolonging their duration of action within the neuronal synapse and the downstream effects of these neurotransmitters. More specifically, bupropion binds to the norepinephrine transporter (NET) and the dopamine transporter (DAT). Bupropion was originally classified as an "atypical" antidepressant because it does not exert the same effects as the classical antidepressants such as Monoamine Oxidase Inhibitors (MAOIs), Tricyclic Antidepressants (TCAs), or Selective Serotonin Reuptake Inhibitors (SSRIs). While it has comparable effectiveness to typical first-line options for the treatment of depression such as SSRIs, bupropion is a unique option for the treatment of MDD as it lacks any clinically relevant serotonergic effects, typical of other mood medications, or any effects on histamine or adrenaline receptors. Lack of activity at these receptors results in a more tolerable side effect profile; bupropion is less likely to cause sexual side effects, sedation, or weight gain as compared to SSRIs or TCAs, for example. When used as an aid to smoking cessation, bupropion is thought to confer its anti-craving and anti-withdrawal effects by inhibiting dopamine reuptake, which is thought to be involved in the reward pathways associated with nicotine, and through the antagonism of the nicotinic acetylcholinergic receptor. A Cochrane Review of meta-analyses of available treatment modalities for smoking cessation found that abstinence rates approximately doubled when bupropion was used as compared to placebo, and was found to have similar rates of smoking cessation as nicotine replacement therapy (NRT). Bupropion is sometimes used as an add-on agent to first-line treatments of depression such as selective serotonin reuptake inhibitor (SSRI) medications when there is a treatment-failure or only partial response. Bupropion is also used off-label for the management of Attention/Deficit-Hyperactivity Disorder (ADHD) in adults with comorbid bipolar depression to avoid mood destabilization caused by typical stimulant medications used for the treatment of ADHD. When used in combination with naltrexone in the marketed product ContraveⓇ for chronic weight management, the two components are thought to have effects on areas of the brain involved in the regulation of food intake. This includes the hypothalamus, which is involved in appetite regulation, and the mesolimbic dopamine circuit, which is involved in reward pathways. Studies have shown that the combined activity of bupropion and naltrexone increase the firing rate of hypothalamic pro-opiomelanocortin (POMC) neurons and blockade of opioid receptor-mediated POMC auto-inhibition, which are associated with a reduction in food intake and increased energy expenditure. The combination of naltrexone and bupropion was shown to result in a statistically significant weight loss, with a mean change in body weight of -6.3% compared to -1.3% for placebo.

Background

Bupropion (also known as the brand name product Wellbutrin®) is a norepinephrine/dopamine-reuptake inhibitor (NDRI) used most commonly for the management of Major Depressive Disorder (MDD), Seasonal Affective Disorder (SAD), and as an aid for smoking cessation. Bupropion exerts its pharmacological effects by weakly inhibiting the enzymes involved in the uptake of the neurotransmitters norepinephrine and dopamine from the synaptic cleft, therefore prolonging their duration of action within the neuronal synapse and the downstream effects of these neurotransmitters. More specifically, bupropion binds to the norepinephrine transporter (NET) and the dopamine transporter (DAT). Bupropion was originally classified as an "atypical" antidepressant because it does not exert the same effects as the classical antidepressants such as Monoamine Oxidase Inhibitors (MAOIs), Tricyclic Antidepressants (TCAs), or Selective Serotonin Reuptake Inhibitors (SSRIs). While it has comparable effectiveness to typical first-line options for the treatment of depression such as SSRIs, bupropion is a unique option for the treatment of MDD as it lacks any clinically relevant serotonergic effects, typical of other mood medications, or any effects on histamine or adrenaline receptors. Lack of activity at these receptors results in a more tolerable side effect profile; bupropion is less likely to cause sexual side effects, sedation, or weight gain as compared to SSRIs or TCAs, for example. When used as an aid to smoking cessation, bupropion is thought to confer its anti-craving and anti-withdrawal effects by inhibiting dopamine reuptake, which is thought to be involved in the reward pathways associated with nicotine, and through the antagonism of the nicotinic acetylcholinergic receptor. A Cochrane Review of meta-analyses of available treatment modalities for smoking cessation found that abstinence rates approximately doubled when bupropion was used as compared to placebo, and was found to have similar rates of smoking cessation as nicotine replacement therapy (NRT). Bupropion is sometimes used as an add-on agent to first-line treatments of depression such as selective serotonin reuptake inhibitor (SSRI) medications when there is a treatment-failure or only partial response. Bupropion is also used off-label for the management of Attention/Deficit-Hyperactivity Disorder (ADHD) in adults with comorbid bipolar depression to avoid mood destabilization caused by typical stimulant medications used for the treatment of ADHD. When used in combination with naltrexone in the marketed product ContraveⓇ for chronic weight management, the two components are thought to have effects on areas of the brain involved in the regulation of food intake. This includes the hypothalamus, which is involved in appetite regulation, and the mesolimbic dopamine circuit, which is involved in reward pathways. Studies have shown that the combined activity of bupropion and naltrexone increase the firing rate of hypothalamic pro-opiomelanocortin (POMC) neurons and blockade of opioid receptor-mediated POMC auto-inhibition, which are associated with a reduction in food intake and increased energy expenditure. The combination of naltrexone and bupropion was shown to result in a statistically significant weight loss, with a mean change in body weight of -6.3% compared to -1.3% for placebo.

Indication

Bupropion is indicated for the treatment of major depressive disorder (MDD), seasonal affective disorder (SAD), and as an aid to smoking cessation. When used in combination with naltrexone as the marketed product ContraveⓇ, bupropion is indicated as an adjunct to a reduced-calorie diet and increased physical activity for chronic weight management in adults with an initial body mass index (BMI) of: 30 kg/m^2 or greater (obese) or 27 kg/m^2 or greater (overweight) in the presence of at least one weight-related comorbid condition (e.g., hypertension, type 2 diabetes mellitus, or dyslipidemia). Bupropion is also used off-label as a first-line treatment in patients with ADHD and comorbid bipolar disorder when used as an adjunct to mood stabilizers.

Associated Conditions

  • Attention Deficit Hyperactivity Disorder (ADHD)
  • Major Depressive Disorder (MDD)
  • Obesity
  • Seasonal Affective Disorder (SAD)

Clinical Trials

Title
Posted
Study ID
Phase
Status
Sponsor
2025/05/15
Phase 1
Active, not recruiting
2025/05/04
Not Applicable
Active, not recruiting
Asad Ullah Jan
2024/11/07
Phase 1
Completed
2024/11/05
Phase 4
Recruiting
2024/09/24
Phase 1
Recruiting
2024/08/22
Not Applicable
Not yet recruiting
2024/08/21
Phase 1
Active, not recruiting
2024/04/18
Phase 1
Recruiting
2024/04/16
Phase 1
Completed
2024/02/12
Phase 4
Recruiting

FDA Drug Approvals

Approved Product
Manufacturer
NDC Code
Route
Strength
Effective Date
Sun Pharmaceutical Industries, Inc.
47335-736
ORAL
100 mg in 1 1
1/10/2023
Bausch Health US LLC
0187-0730
ORAL
150 mg in 1 1
3/4/2022
CIPLA USA INC.,
69097-917
ORAL
75 mg in 1 1
3/27/2023
STAT Rx USA LLC
16590-246
ORAL
300 mg in 1 1
8/22/2012
NuCare Pharmaceuticals,Inc.
68071-2577
ORAL
100 mg in 1 1
7/17/2023
Chartwell RX, LLC
62135-875
ORAL
150 mg in 1 1
4/5/2024
Lupin Pharmaceuticals, Inc.
68180-320
ORAL
300 mg in 1 1
4/19/2023
AvPAK
50268-142
ORAL
75 mg in 1 1
1/9/2024
Actavis Pharma, Inc.
0591-3543
ORAL
150 mg in 1 1
3/21/2023
REMEDYREPACK INC.
70518-2641
ORAL
100 mg in 1 1
3/24/2025

EMA Drug Approvals

Approved Product
Authorization Holder
Status
Issued Date
Authorised
3/26/2015

HSA Drug Approvals

Approved Product
Manufacturer
Approval Number
Dosage Form
Strength
Approval Date
WELLBUTRIN SR TABLETS 150 mg
SIN10983P
TABLET, FILM COATED
150 mg
6/16/1999
CONTRAVE PROLONGED RELEASE TABLET 8MG/90MG
SIN16411P
TABLET, FILM COATED, EXTENDED RELEASE
90mg
1/3/2022

NMPA Drug Approvals

Approved Product
Company
Approval Number
Drug Type
Dosage Form
Approval Date
Bupropion Hydrochloride Tablets
国药准字H20051823
化学药品
片剂
6/30/2020
Bupropion Hydrochloride Tablets
国药准字H20070209
化学药品
片剂
11/15/2021
Bupropion Hydrochloride Sustained-release Tablets
国药准字H20203582
化学药品
片剂
11/17/2020
Bupropion Hydrochloride Sustained-release Tablets
国药准字H20080111
化学药品
片剂
2/14/2023
Bupropion Hydrochloride Sustained-release Tablets
国药准字H20090221
化学药品
片剂
5/22/2019
Bupropion Hydrochloride Sustained-release Tablets
国药准字H20080398
化学药品
片剂
10/12/2021
Bupropion Hydrochloride Sustained-release Tablets
国药准字H20203581
化学药品
片剂
11/17/2020
Bupropion Hydrochloride Sustained-release Tablets
国药准字H20055847
化学药品
片剂
8/17/2020
Bupropion Hydrochloride Sustained-release Tablets
国药准字H20203580
化学药品
片剂
11/17/2020
Bupropion Hydrochloride Sustained-release Tablets
国药准字H20080344
化学药品
片剂
12/22/2022

PPB Drug Approvals

Approved Product
Registration No.
Company
Licence No.
Strength
Registration Date
WELLBUTRIN XL EXTENDED RELEASE TAB 300 MG
N/A
N/A
N/A
8/21/2009
CONTRAVE PROLONGED-RELEASE TABLETS 8MG/90MG
N/A
N/A
N/A
12/10/2020
WELLBUTRIN XL EXTENDED RELEASE TAB 150MG
N/A
N/A
N/A
9/14/2009
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