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Approved Marketing Authorisations (MA) containing Bupropion in Europe. Original Data : EMA Website

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Product

Bupropion
Bupropion Hydrobromide
CAS 34911-51-8
Europe

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Bora Pharmaceuticals- Making success more certain.

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Polfa Tarchomin is a leading Polish pharmaceutical company with 200 year tradition in manufacture and sale of pharmaceutical products.

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Axplora- The partner of choice for complex APIs.

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Fareva is a one-stop-shop for API/HPAPI, OSD & Sterile products, is USFDA, EMA and PMDA-inspected and has multiple NDA & ANDA filings.

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Bupropion

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CHEMISTRY
Discover Molecule Insights

ACTIVE PHARMA INGREDIENTS

58 API Suppliers, 37 USDMF, 10 EU WC, 8 KDMF, 33 NDC API, 34 Listed Suppliers, $ API Reference Price

58 API Suppliers
37 USDMF
10 EU WC
8 KDMF
33 NDC API
34 Listed Suppliers
$ API Reference Price

DEVELOPMENTS

29 Drugs in Development

29 Drugs in Development

PRICE INFORMATION

API Reference Price, API Exports, API Imports, FDF Imports

API Reference Price
API Exports
API Imports
FDF Imports

INTERMEDIATES

5 API Suppliers

5 API Suppliers

FINISHED DOSAGE FORMULATIONS

264 FDF Dossiers, 130 FDA Orange Book, 85 Europe, 12 Canada, 2 Australia, 17 South Africa, 18 Listed Dossiers

264 FDF Dossiers
130 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TABLET;ORAL - 100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, TABLET;ORAL - 50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, TABLET;ORAL - 75MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, TABLET, EXTENDED RELEASE;ORAL - 90MG;8MG, TABLET, EXTENDED RELEASE;ORAL - 100MG, TABLET, EXTENDED RELEASE;ORAL - 150MG,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- 200MG, TABLET, EXTENDED RELEASE;ORAL - 150MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, TABLET, EXTENDED RELEASE;ORAL - 150MG, TABLET, EXTENDED RELEASE;ORAL - 300MG, TABLET, EXTENDED RELEASE;ORAL - 450MG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, 10 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, 23 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 Coloring Agents, 5 Empty Capsules, 5 Surfactant & Foaming 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
23 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 Coloring Agents
5 Empty Capsules
5 Surfactant & Foaming 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

Filters

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Filters

FILTER :

filter Applicant Reset all filters

85 All

01 2Orion Corporation

02 12care4

03 62care4 ApS

04 1BB FARMA SRL

05 1Cross Pharma AB

06 1DOC GENERICI SRL

07 3Farm Agon

08 2GLAXOSMITHKLINE SPA

09 6GLAXOSMITHKLINE SpA

10 1GMM FARMA SRL

11 1GlaxoSmithKline

12 2GlaxoSmithKline AB

13 4GlaxoSmithKline AG

14 5GlaxoSmithKline leads AS

15 7Medartuum AB

16 2Omnia Läkemedel AB

17 7Omnia Pharmaceutical AB

18 1Orexigen Therapeutics Ireland Limited (1)

19 25Orifarm AB

20 1Orifarm AS

21 1Paranova Pharmaceutical AB

22 1SANDOZ SPA

23 2Sandoz A / S,

24 1TEVA BV

25 1Torrent Pharma, Inc.

filter Active Ingredients Reset all filters

85 All

01 23Bupropion

02 4Bupropion hydrochloride

03 2Naltreksonhydrochloride, Bupropionhydrochloride

04 1Naltreksonhydrochloride; Bupropionhydrochloride

05 36bupropion hydrochloride

06 19bupropionhydroklorid

filter Dosage Form Reset all filters

85 All

01 6Antic-calc tablet Modified Release

02 2Bupropion 150Mg 30 Joined' Oral Use Rp

03 2Bupropion 300Mg 30 Joined' Oral Use Rp

04 3Depot tablet

05 3Depottablett

06 26MODIFIED-RELEASE TABLET

07 7Modified Release Tablets

08 10PROLONGED-RELEASE TABLET

09 4Ret Tabl

10 1SR TABLET

11 19TABLETT MED MODIFIERAD FRISÄTTNING

12 2Blank

filter Country Reset all filters

85 All

01 13Italy

02 12Norway

03 55Sweden

04 4Switzerland

05 1United Kingdom

filter Brand Name Reset all filters

85 All

01 1BUPROPION DOC

02 1BUPROPION SANDOZ

03 1BUPROPION TEVA

04 2Bupropion Orion

05 1Bupropion Paranova

06 2Bupropion Sandoz

07 1ELONTRIL

08 2Elontril

09 3Mysimba

10 19Voxra

11 3WELLBUTRIN

12 24Wellbutrin

13 6Wellbutrin Retard

14 2Wellbutrin XR

15 16Zyban

16 1Blank

FDF Dossiers
FDA Orange Book
Europe
Canada
Australia
South Africa
Listed Dossiers

List of Suppliers

Product Main Page

01

Orion Corporation

FNCE 2024

Not Confirmed

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Digital Content

Regulatory Info :

Registration Country : Sweden

bupropion hydrochloride

Brand Name : Bupropion Orion

Dosage Form : MODIFIED-RELEASE TABLET

Dosage Strength : 150 MG

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Sweden

Fermion Orion Company Banner

Portfolio PDF

Product Web Link

Digital Content

Corporate PDF

02

Orion Corporation

FNCE 2024

Not Confirmed

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Digital Content

Regulatory Info :

Registration Country : Sweden

bupropion hydrochloride

Brand Name : Bupropion Orion

Dosage Form : MODIFIED-RELEASE TABLET

Dosage Strength : 300 MG

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Sweden

Fermion Orion Company Banner

Portfolio PDF

Product Web Link

Digital Content

Corporate PDF

03

Orifarm AB

FNCE 2024

Not Confirmed

Orifarm AB

FNCE 2024

Not Confirmed

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Digital Content

Regulatory Info :

Registration Country : Sweden

bupropionhydroklorid

Brand Name : Voxra

Dosage Form : TABLETT MED MODIFIERAD FRISÄTTNING

Dosage Strength : 150 MG

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Sweden

Portfolio PDF

Product Web Link

Digital Content

Corporate PDF

04

Orifarm AB

FNCE 2024

Not Confirmed

Orifarm AB

FNCE 2024

Not Confirmed

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Digital Content

Regulatory Info :

Registration Country : Sweden

bupropionhydroklorid

Brand Name : Voxra

Dosage Form : TABLETT MED MODIFIERAD FRISÄTTNING

Dosage Strength : 150 MG

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Sweden

Portfolio PDF

Product Web Link

Digital Content

Corporate PDF

05

Orifarm AB

FNCE 2024

Not Confirmed

Orifarm AB

FNCE 2024

Not Confirmed

Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.

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Digital Content

Regulatory Info :

Registration Country : Sweden

bupropionhydroklorid

Brand Name : Voxra

Dosage Form : TABLETT MED MODIFIERAD FRISÄTTNING

Dosage Strength : 150 MG

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Sweden

Portfolio PDF

Product Web Link

Digital Content

Corporate PDF

06

Orifarm AB

FNCE 2024

Not Confirmed

Orifarm AB

FNCE 2024

Not Confirmed

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Digital Content

Regulatory Info :

Registration Country : Sweden

bupropionhydroklorid

Brand Name : Voxra

Dosage Form : TABLETT MED MODIFIERAD FRISÄTTNING

Dosage Strength : 150 MG

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Sweden

Portfolio PDF

Product Web Link

Digital Content

Corporate PDF

07

Paranova Pharmaceutical AB

FNCE 2024

Not Confirmed

Paranova Pharmaceutical AB

FNCE 2024

Not Confirmed

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Digital Content

Regulatory Info :

Registration Country : Sweden

bupropion hydrochloride

Brand Name : Bupropion Paranova

Dosage Form : PROLONGED-RELEASE TABLET

Dosage Strength : 150 MG

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Sweden

Portfolio PDF

Product Web Link

Digital Content

Corporate PDF

08

Sandoz A / S,

FNCE 2024

Not Confirmed

Sandoz A / S,

FNCE 2024

Not Confirmed

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Digital Content

Regulatory Info :

Registration Country : Sweden

bupropion hydrochloride

Brand Name : Bupropion Sandoz

Dosage Form : MODIFIED-RELEASE TABLET

Dosage Strength : 150 MG

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Sweden

Product Web Link

Digital Content

09

Sandoz A / S,

FNCE 2024

Not Confirmed

Sandoz A / S,

FNCE 2024

Not Confirmed

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Digital Content

Regulatory Info :

Registration Country : Sweden

bupropion hydrochloride

Brand Name : Bupropion Sandoz

Dosage Form : MODIFIED-RELEASE TABLET

Dosage Strength : 300 MG

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Sweden

Product Web Link

Digital Content

10

Torrent Pharma, Inc.

FNCE 2024

Not Confirmed

Torrent Pharma, Inc.

FNCE 2024

Not Confirmed

Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.

Post an Enquiry

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Digital Content

Regulatory Info : Generic

Registration Country : United Kingdom

Brand Name :

Dosage Form : SR TABLET

Dosage Strength : 10MG

Packaging :

Approval Date :

Application Number :

Regulatory Info : Generic

Registration Country : United Kingdom

Portfolio PDF

Product Web Link

Digital Content

Corporate PDF

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