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Nemexin
Europe

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Naltrexone HCL

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Mission CDMO team brings reliability, resourcefulness, & responsiveness in executing your development project.

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Naltrexone Hydrochloride

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pharmacompass-2-2026-02-09

Nemexin

ACCESS ALL DATA, CHEMISTRY

ACCESS ALL DATA
CHEMISTRY
Discover Molecule Insights

ACTIVE PHARMA INGREDIENTS

73 API Suppliers, 8 USDMF, 8 CEP/COS, 2 EU WC, 8 KDMF, 54 NDC API, 21 Listed Suppliers, $ API Reference Price

73 API Suppliers
8 USDMF
8 CEP/COS
2 EU WC
8 KDMF
54 NDC API
21 Listed Suppliers
$ API Reference Price

DEVELOPMENTS

18 Drugs in Development

18 Drugs in Development

INTERMEDIATES

2 Intermediate Suppliers

2 Intermediate Suppliers

FINISHED DOSAGE FORMULATIONS

46 FDF Dossiers, 23 FDA Orange Book, 13 Europe, 4 Canada, 2 South Africa, 4 Listed Dossiers

46 FDF Dossiers
23 FDA Orange Book
13 Europe
4 Canada
2 South Africa
4 Listed Dossiers

DRUG PRODUCT COMPOSITIONS

TABLET, EXTENDED RELEASE;ORAL - 90MG;8MG, CAPSULE, EXTENDED RELEASE;ORAL - 100MG;4MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, CAPSULE, EXTENDED RELEASE;ORAL - 20MG;0.8MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, CAPSULE, EXTENDED RELEASE;ORAL - 30MG;1.2MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, CAPSULE, EXTENDED RELEASE;ORAL - 50MG;2MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, CAPSULE, EXTENDED RELEASE;ORAL - 60MG;2.4MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, CAPSULE, EXTENDED RELEASE;ORAL - 80MG;3.2MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

TABLET, EXTENDED RELEASE;ORAL - 90MG;8MG
CAPSULE, EXTENDED RELEASE;ORAL - 100MG;4MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
CAPSULE, EXTENDED RELEASE;ORAL - 20MG;0.8MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
CAPSULE, EXTENDED RELEASE;ORAL - 30MG;1.2MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
CAPSULE, EXTENDED RELEASE;ORAL - 50MG;2MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
CAPSULE, EXTENDED RELEASE;ORAL - 60MG;2.4MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
CAPSULE, EXTENDED RELEASE;ORAL - 80MG;3.2MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

RELATED EXCIPIENT COMPANIES

3 Evonik, 1 SPI Pharma, 4 Gangwal Healthcare, 3 Nanjing Well Pharmaceutical, 1 Pfanstiehl, 5 Kirsch Pharma, 4 ACG Worldwide, 8 Actylis, 1 Aeon Procare, 1 Alcedo Pharmachem, 6 Anhui Sunhere Pharmaceutical Excipients Co.,Ltd, 17 BASF, 1 CD Formulation, 1 Clariant, 18 Corel Pharma Chem, 6 DFE Pharma, 1 Esteem Industries, 1 Finar, 10 Gangwal Chemicals, 1 Gloria Interchem, 8 Ideal Cures, 1 Ingredion Pharma Solutions, 23 Kerry, 2 Keval Exports, 4 Kima Chemical, 6 Lonza Capsugel, 11 Microlex e.U, 1 Nanjing Bold Chemical, 1 Neelkanth MineChem, 2 Nitika Pharmaceutical Specialities, 2 Nomisma Healthcare, 1 Novo Excipients, 1 Pharmatrans-Sanaq, 4 Pluviaendo, 3 Prachin Chemical, 1 Qianhao Chemical (Hebei) Co., Ltd, 2 Qualicaps, 10 Roquette, 12 Seppic, 4 Shanghai Shenmei Pharmaceutical Technology Co., Ltd, 10 Sigachi Industries, 3 Silverline Chemicals, 3 The Dow Chemical Company, 1 Valens Pharmachem, 3 Vasa Pharmachem, 1 Vertellus

EXCIPIENTS BY APPLICATIONS

57 Coating Systems & Additives, 36 Controlled & Modified Release, 34 Fillers, Diluents & Binders, 24 Granulation, 23 Thickeners and Stabilizers, 22 Direct Compression, 19 Solubilizers, 14 Parenteral, 14 Lubricants & Glidants, 14 Disintegrants & Superdisintegrants, 13 Topical, 12 Film Formers & Plasticizers, 11 Taste Masking, 9 Co-Processed Excipients, 9 Empty Capsules, 7 Emulsifying Agents, 5 Rheology Modifiers, 5 Surfactant & Foaming Agents, 5 API Stability Enhancers, 4 Chewable & Orodispersible Aids, 4 Vegetarian Capsules, 2 Coloring Agents

57 Coating Systems & Additives
36 Controlled & Modified Release
34 Fillers, Diluents & Binders
24 Granulation
23 Thickeners and Stabilizers
22 Direct Compression
19 Solubilizers
14 Parenteral
14 Lubricants & Glidants
14 Disintegrants & Superdisintegrants
13 Topical
12 Film Formers & Plasticizers
11 Taste Masking
9 Co-Processed Excipients
9 Empty Capsules
7 Emulsifying Agents
5 Rheology Modifiers
5 Surfactant & Foaming Agents
5 API Stability Enhancers
4 Chewable & Orodispersible Aids
4 Vegetarian Capsules
2 Coloring Agents

DIGITAL CONTENT

1 Data Compilation #PharmaFlow, 49 News #PharmaBuzz

1 Data Compilation #PharmaFlow
49 News #PharmaBuzz

GLOBAL SALES INFORMATION

12 US Medicaid Prescriptions, 12 Regulatory FDF Prices

12 US Medicaid Prescriptions
12 Regulatory FDF Prices

MARKET PLACE

18 APIs, 3 FDF Dossiers

18 APIs
3 FDF Dossiers

PATENTS & EXCLUSIVITIES

66 US Patents, 4 Health Canada Patents

66 US Patents
4 Health Canada Patents

REF. STANDARDS & IMPURITIES

2 EDQM, 7 Others

2 EDQM
7 Others

$ API Ref.Price (USD/KG) : 6,454 Xls

Filters

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filter Applicant Reset all filters

13 All

01 12care4 ApS

02 1ACCORD HEALTHCARE LIMITED

03 1Accord Healthcare Slu

04 1Bristol-Myers Squibb

05 1MOLTENI & C. F.LLI ALITTI SpA

06 3Orexigen Therapeutics Ireland Limited

07 1Orexigen Therapeutics Ireland Limited (1)

08 1Orifarm AS

09 1SIRTON MEDICARE Srl

10 2ZAMBON ITALIA Srl

filter Active Ingredients Reset all filters

13 All

01 2Bupropion Hydrochloride; Naltrexone Hydrochloride

02 7Naltrexone Hydrochloride

03 1Naltrexone Hydrochloride; Bupropion Hydrochloride

04 3Naltrexone Hydrochloride; Bupropion hydrochloride

filter Dosage Form Reset all filters

13 All

01 1Extended-Release Tablet

02 2Film Coated Tablet

03 2Naltrexone 50Mg 10 Units Oral Use

04 3Naltrexone 50Mg 14 Joined' Oral Use

05 1Prolonged-Release Tablet

06 4Tablet

filter Country Reset all filters

13 All

01 1Denmark

02 5Italy

03 3Norway

04 3Spain

05 1Sweden

filter Brand Name Reset all filters

13 All

01 2Antaxone

02 6Mysimba

03 1Nalorex

04 1Naltrexone

05 1Narcoral

06 1Revia Coated Tablets

07 1Tranalex

Naltrexone Hydrochloride

List of Suppliers

Product Main Page

01

2care4 ApS

Natural Product Expo West

Not Confirmed

2care4 ApS

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Regulatory Info : Marketed

Registration Country : Norway

Naltrexone Hydrochloride; Bupropion hydrochloride

Brand Name : Mysimba

Dosage Form : Tablet

Dosage Strength : 8mg; 90mg

Packaging :

Approval Date :

Application Number :

Regulatory Info : Marketed

Registration Country : Norway

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Digital Content

Corporate PDF

02

ACCORD HEALTHCARE LIMITED

Clinical Outsourcing

Not Confirmed

ACCORD HEALTHCARE LIMITED

Clinical Outsourcing

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Regulatory Info :

Registration Country : Italy

Naltrexone Hydrochloride

Brand Name : Naltrexone

Dosage Form : Naltrexone 50Mg 14 Joined' Oral Use

Dosage Strength : 14 cpr riv 50 mg

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Italy

Portfolio PDF

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03

Accord Healthcare Slu

Clinical Outsourcing

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Accord Healthcare Slu

Clinical Outsourcing

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Regulatory Info : Authorized

Registration Country : Spain

Naltrexone Hydrochloride

Brand Name : Tranalex

Dosage Form : Film Coated Tablet

Dosage Strength : 50MG

Packaging :

Approval Date : 25-04-2011

Application Number : 73938

Regulatory Info : Authorized

Registration Country : Spain

Portfolio PDF

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Corporate PDF

04

Bristol-Myers Squibb

Clinical Outsourcing

Not Confirmed

Bristol-Myers Squibb

Clinical Outsourcing

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Regulatory Info : Authorized

Registration Country : Spain

Naltrexone Hydrochloride

Brand Name : Revia Coated Tablets

Dosage Form : Film Coated Tablet

Dosage Strength :

Packaging :

Approval Date : 18-11-2004

Application Number : 3417516

Regulatory Info : Authorized

Registration Country : Spain

Portfolio PDF

Product Web Link

Digital Content

Corporate PDF

05

MOLTENI & C. F.LLI ALITTI SpA

Clinical Outsourcing

Not Confirmed

MOLTENI & C. F.LLI ALITTI SpA

Clinical Outsourcing

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Digital Content

Regulatory Info :

Registration Country : Italy

Naltrexone Hydrochloride

Brand Name : Nalorex

Dosage Form : Naltrexone 50Mg 14 Joined' Oral Use

Dosage Strength : 14 cpr riv 50 mg

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Italy

Portfolio PDF

Product Web Link

Digital Content

Corporate PDF

06

Orifarm AS

Clinical Outsourcing

Not Confirmed

Orifarm AS

Clinical Outsourcing

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Digital Content

Regulatory Info : Not Marketed

Registration Country : Norway

Naltrexone Hydrochloride; Bupropion hydrochloride

Brand Name : Mysimba

Dosage Form : Tablet

Dosage Strength : 8mg; 90mg

Packaging :

Approval Date :

Application Number :

Regulatory Info : Not Marketed

Registration Country : Norway

Portfolio PDF

Product Web Link

Digital Content

Corporate PDF

07

Orexigen Therapeutics Ireland Limited (1...

Country

Natural Product Expo West

Not Confirmed

Orexigen Therapeutics Ireland Limited (1...

Country

Natural Product Expo West

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Country

Virtual Booth

Digital Content

Regulatory Info : Marketed

Registration Country : Norway

Naltrexone Hydrochloride; Bupropion hydrochloride

Brand Name : Mysimba

Dosage Form : Tablet

Dosage Strength : 8mg; 90mg

Packaging :

Approval Date :

Application Number :

Regulatory Info : Marketed

Registration Country : Norway

Portfolio PDF

Product Web Link

Virtual Booth

Digital Content

Website

Corporate PDF

08

Orexigen Therapeutics Ireland Limited

Country

Natural Product Expo West

Not Confirmed

Orexigen Therapeutics Ireland Limited

Country

Natural Product Expo West

Not Confirmed

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Regulatory Info : Authorized

Registration Country : Spain

Naltrexone Hydrochloride; Bupropion Hydrochloride

Brand Name : Mysimba

Dosage Form : Extended-Release Tablet

Dosage Strength : 8MG; 90 MG

Packaging :

Approval Date : 10-10-2016

Application Number : 114988001

Regulatory Info : Authorized

Registration Country : Spain

Portfolio PDF

Product Web Link

Virtual Booth

Digital Content

Website

Corporate PDF

09

Orexigen Therapeutics Ireland Limited

Country

Natural Product Expo West

Not Confirmed

Orexigen Therapeutics Ireland Limited

Country

Natural Product Expo West

Not Confirmed

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Country

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Regulatory Info : Prescription

Registration Country : Denmark

Bupropion Hydrochloride; Naltrexone Hydrochloride

Brand Name : Mysimba

Dosage Form : Prolonged-Release Tablet

Dosage Strength : 8mg; 90mg

Packaging :

Approval Date : 26-03-2015

Application Number : 28105317313

Regulatory Info : Prescription

Registration Country : Denmark

Portfolio PDF

Product Web Link

Virtual Booth

Digital Content

Website

Corporate PDF

10

Orexigen Therapeutics Ireland Limited

Country

Natural Product Expo West

Not Confirmed

Orexigen Therapeutics Ireland Limited

Country

Natural Product Expo West

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Regulatory Info : Approved

Registration Country : Sweden

Bupropion Hydrochloride; Naltrexone Hydrochloride

Brand Name : Mysimba

Dosage Form : Tablet

Dosage Strength : 8mg;90mg

Packaging :

Approval Date : 26-03-2015

Application Number : 2.01E+13

Regulatory Info : Approved

Registration Country : Sweden

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Digital Content

Website

Corporate PDF

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Product listings are provided for informational purposes only. We do not supply or sell any products. Any products that may be covered by patent(s) are supplied solely for uses permitted under Section 107A of the Indian Patents Act and not for commercial sale.