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Bupropion
Canada

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Bupropion

ACCESS ALL DATA, CHEMISTRY

ACCESS ALL DATA
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CHEMISTRY
Discover Molecule Insights

ACTIVE PHARMA INGREDIENTS

60 API Suppliers, 38 USDMF, 10 EU WC, 8 KDMF, 33 NDC API, 35 Listed Suppliers, $ API Reference Price

60 API Suppliers
38 USDMF
10 EU WC
8 KDMF
33 NDC API
35 Listed Suppliers
$ API Reference Price

DEVELOPMENTS

29 Drugs in Development

29 Drugs in Development

INTERMEDIATES

5 Intermediates Suppliers

5 Intermediates Suppliers

FINISHED DOSAGE FORMULATIONS

267 FDF Dossiers, 133 FDA Orange Book, 85 Europe, 12 Canada, 2 Australia, 17 South Africa, 18 Listed Dossiers

267 FDF Dossiers
133 FDA Orange Book
85 Europe
12 Canada
2 Australia
17 South Africa
18 Listed Dossiers

DRUG PRODUCT COMPOSITIONS

TABLET;ORAL - 100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, TABLET;ORAL - 50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, TABLET;ORAL - 75MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, TABLET, EXTENDED RELEASE;ORAL - 90MG;8MG, TABLET, EXTENDED RELEASE;ORAL - 100MG, TABLET, EXTENDED RELEASE;ORAL - 150MG, TABLET, EXTENDED RELEASE;ORAL - 200MG, TABLET, EXTENDED RELEASE;ORAL - 150MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, TABLET, EXTENDED RELEASE;ORAL - 150MG, TABLET, EXTENDED RELEASE;ORAL - 300MG, TABLET, EXTENDED RELEASE;ORAL - 450MG

TABLET;ORAL - 100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
TABLET;ORAL - 50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
TABLET;ORAL - 75MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
TABLET, EXTENDED RELEASE;ORAL - 90MG;8MG
TABLET, EXTENDED RELEASE;ORAL - 100MG
TABLET, EXTENDED RELEASE;ORAL - 150MG
TABLET, EXTENDED RELEASE;ORAL - 200MG
TABLET, EXTENDED RELEASE;ORAL - 150MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
TABLET, EXTENDED RELEASE;ORAL - 150MG
TABLET, EXTENDED RELEASE;ORAL - 300MG
TABLET, EXTENDED RELEASE;ORAL - 450MG

RELATED EXCIPIENT COMPANIES

1 Minakem, 2 Evonik, 2 Rochem International Inc, 19 SPI Pharma, 2 Seqens, 14 DKSH, 2 Jai Radhe Sales, 3 Boai NKY Pharmaceuticals Ltd, 1 Chynops Pharma, 12 Gangwal Healthcare, 9 Nanjing Well Pharmaceutical, 1 Pfanstiehl, 1 ACG Worldwide, 6 Actylis, 1 Aeon Procare, 4 Alcedo Pharmachem, 8 Anhui Sunhere Pharmaceutical Excipients Co.,Ltd, 35 BASF, 2 Clariant, 16 Corel Pharma Chem, 5 DFE Pharma, 3 Doshion Polyscience, 3 Finar, 12 Gangwal Chemicals, 1 Huzhou Sunflower Pharmaceutical, 15 Ideal Cures Pvt Ltd, 3 Ingredion Pharma Solutions, 39 Kerry, 5 Kima Chemical, 6 Lonza Capsugel, 21 Microlex e.U, 1 Nanjing Bold Chemical, 1 NEWEDGE Overseas, 2 Nomisma Healthcare, 4 Novo Excipients, 3 Pharmatrans-Sanaq, 7 Pluviaendo, 3 Prachin Chemical, 1 Qianhao Chemical (Hebei) Co., Ltd, 1 Qualicaps, 19 Roquette, 14 Seppic, 5 Shanghai Shenmei Pharmaceutical Technology Co., Ltd, 1 Shijiazhuang Huaxu Pharmaceutical, 10 Sigachi Industries, 4 The Dow Chemical Company, 1 Ulanqab Kema New Material, 2 Valens Pharmachem, 2 Vasa Pharmachem, 2 Vertellus

EXCIPIENTS BY APPLICATIONS

105 Fillers, Diluents & Binders, 80 Coating Systems & Additives, 51 Controlled & Modified Release, 48 Direct Compression, 36 Solubilizers, 31 Lubricants & Glidants, 30 Granulation, 30 Thickeners and Stabilizers, 29 Film Formers & Plasticizers, 27 Taste Masking, 22 Parenteral, 21 Topical, 19 Co-Processed Excipients, 18 Disintegrants & Superdisintegrants, 17 Chewable & Orodispersible Aids, 11 Emulsifying Agents, 8 API Stability Enhancers, 7 Rheology Modifiers, 5 Empty Capsules, 5 Surfactant & Foaming Agents, 5 Coloring Agents, 4 Vegetarian Capsules

105 Fillers, Diluents & Binders
80 Coating Systems & Additives
51 Controlled & Modified Release
48 Direct Compression
36 Solubilizers
31 Lubricants & Glidants
30 Granulation
30 Thickeners and Stabilizers
29 Film Formers & Plasticizers
27 Taste Masking
22 Parenteral
21 Topical
19 Co-Processed Excipients
18 Disintegrants & Superdisintegrants
17 Chewable & Orodispersible Aids
11 Emulsifying Agents
8 API Stability Enhancers
7 Rheology Modifiers
5 Empty Capsules
5 Surfactant & Foaming Agents
5 Coloring Agents
4 Vegetarian Capsules

DIGITAL CONTENT

4 DATA COMPILATION #PharmaFlow, 90 NEWS #PharmaBuzz

4 DATA COMPILATION #PharmaFlow
90 NEWS #PharmaBuzz

GLOBAL SALES INFORMATION

6 US Medicaid Prescriptions, 62 Finished Drug Prices, 10 Annual Reports

6 US Medicaid Prescriptions
62 Finished Drug Prices
10 Annual Reports

MARKET PLACE

10 APIs, 2 FDF Dossiers

10 APIs
2 FDF Dossiers

PATENTS & EXCLUSIVITIES

23 US Patents, 30 Health Canada Patents

23 US Patents
30 Health Canada Patents

REF. STANDARDS & IMPURITIES

5 USP, 8 Others

5 USP
8 Others

ANALYTICAL

2 BioAnalytical Methods

2 BioAnalytical Methods

$ API Ref.Price (USD/KG) : 63 Xls

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12 All

01 4BAUSCH HEALTH, CANADA INC.

02 2ODAN LABORATORIES LTD

03 2Pharmascience Inc.

04 2SUN PHARMA CANADA INC

05 2TEVA CANADA LIMITED

filter Active Ingredients Reset all filters

12 All

01 10BUPROPION HYDROCHLORIDE

02 2Bupropion Hydrochloride

filter Dosage Form Reset all filters

12 All

01 12TABLET (EXTENDED-RELEASE)

filter Brand Name Reset all filters

12 All

01 1CONTRAVE

02 2ODAN BUPROPION SR

03 2PMS-BUPROPION SR

04 2TARO-BUPROPION XL

05 2TEVA-BUPROPION XL

06 2WELLBUTRIN XL

07 1ZYBAN

List of Suppliers

Product Main Page

01

BAUSCH HEALTH, CANADA INC.

Compamed

Not Confirmed

BAUSCH HEALTH, CANADA INC.

Compamed

Not Confirmed

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Digital Content

Regulatory Info : Prescription

Registration Country : Canada

BUPROPION HYDROCHLORIDE

Brand Name : ZYBAN

Dosage Form : TABLET (EXTENDED-RELEASE)

Dosage Strength : 150MG

Packaging :

Approval Date :

Application Number : 2238441

Regulatory Info : Prescription

Registration Country : Canada

Portfolio PDF

Product Web Link

Digital Content

Corporate PDF

02

BAUSCH HEALTH, CANADA INC.

Compamed

Not Confirmed

BAUSCH HEALTH, CANADA INC.

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Digital Content

Regulatory Info : Prescription

Registration Country : Canada

BUPROPION HYDROCHLORIDE

Brand Name : WELLBUTRIN XL

Dosage Form : TABLET (EXTENDED-RELEASE)

Dosage Strength : 150MG

Packaging :

Approval Date :

Application Number : 2275090

Regulatory Info : Prescription

Registration Country : Canada

Portfolio PDF

Product Web Link

Digital Content

Corporate PDF

03

BAUSCH HEALTH, CANADA INC.

Compamed

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BAUSCH HEALTH, CANADA INC.

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Digital Content

Regulatory Info : Prescription

Registration Country : Canada

BUPROPION HYDROCHLORIDE

Brand Name : WELLBUTRIN XL

Dosage Form : TABLET (EXTENDED-RELEASE)

Dosage Strength : 300MG

Packaging :

Approval Date :

Application Number : 2275104

Regulatory Info : Prescription

Registration Country : Canada

Portfolio PDF

Product Web Link

Digital Content

Corporate PDF

04

BAUSCH HEALTH, CANADA INC.

Compamed

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BAUSCH HEALTH, CANADA INC.

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Digital Content

Regulatory Info : Prescription

Registration Country : Canada

BUPROPION HYDROCHLORIDE

Brand Name : CONTRAVE

Dosage Form : TABLET (EXTENDED-RELEASE)

Dosage Strength : 90MG

Packaging : 70/120

Approval Date :

Application Number : 2472945

Regulatory Info : Prescription

Registration Country : Canada

Portfolio PDF

Product Web Link

Digital Content

Corporate PDF

05

ODAN LABORATORIES LTD

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ODAN LABORATORIES LTD

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Digital Content

Regulatory Info : Prescription

Registration Country : Canada

BUPROPION HYDROCHLORIDE

Brand Name : ODAN BUPROPION SR

Dosage Form : TABLET (EXTENDED-RELEASE)

Dosage Strength : 100MG

Packaging :

Approval Date :

Application Number : 2275074

Regulatory Info : Prescription

Registration Country : Canada

Portfolio PDF

Product Web Link

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06

ODAN LABORATORIES LTD

Compamed

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ODAN LABORATORIES LTD

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Digital Content

Regulatory Info : Prescription

Registration Country : Canada

BUPROPION HYDROCHLORIDE

Brand Name : ODAN BUPROPION SR

Dosage Form : TABLET (EXTENDED-RELEASE)

Dosage Strength : 150MG

Packaging :

Approval Date :

Application Number : 2275082

Regulatory Info : Prescription

Registration Country : Canada

Portfolio PDF

Product Web Link

Digital Content

Corporate PDF

07

Pharmascience Inc.

Compamed

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Pharmascience Inc.

Compamed

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Digital Content

Regulatory Info : Prescription

Registration Country : Canada

Bupropion Hydrochloride

Brand Name : PMS-BUPROPION SR

Dosage Form : TABLET (EXTENDED-RELEASE)

Dosage Strength : 100MG

Packaging : 60

Approval Date :

Application Number :

Regulatory Info : Prescription

Registration Country : Canada

Portfolio PDF

Product Web Link

Digital Content

08

Pharmascience Inc.

Compamed

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Pharmascience Inc.

Compamed

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Digital Content

Regulatory Info : Prescription

Registration Country : Canada

Bupropion Hydrochloride

Brand Name : PMS-BUPROPION SR

Dosage Form : TABLET (EXTENDED-RELEASE)

Dosage Strength : 150MG

Packaging : 100/500

Approval Date :

Application Number :

Regulatory Info : Prescription

Registration Country : Canada

Portfolio PDF

Product Web Link

Digital Content

09

SUN PHARMA CANADA INC

Compamed

Not Confirmed

SUN PHARMA CANADA INC

Compamed

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Digital Content

Regulatory Info : Prescription

Registration Country : Canada

BUPROPION HYDROCHLORIDE

Brand Name : TARO-BUPROPION XL

Dosage Form : TABLET (EXTENDED-RELEASE)

Dosage Strength : 150MG

Packaging : 30/500

Approval Date :

Application Number : 2475804

Regulatory Info : Prescription

Registration Country : Canada

Portfolio PDF

Product Web Link

Digital Content

Corporate PDF

10

SUN PHARMA CANADA INC

Compamed

Not Confirmed

SUN PHARMA CANADA INC

Compamed

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Digital Content

Regulatory Info : Prescription

Registration Country : Canada

BUPROPION HYDROCHLORIDE

Brand Name : TARO-BUPROPION XL

Dosage Form : TABLET (EXTENDED-RELEASE)

Dosage Strength : 300MG

Packaging : 30/500

Approval Date :

Application Number : 2475812

Regulatory Info : Prescription

Registration Country : Canada

Portfolio PDF

Product Web Link

Digital Content

Corporate PDF

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