Naltrexone Hydrochloride | Health Canada | Drug Product Database | DPD | PharmaCompass.com

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Naltrexone Hydrochloride
Canada

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Faran Shimi Naltrexone Hydrochloride

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Naltrexone Hydrochloride

ACCESS ALL DATA, CHEMISTRY

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CHEMISTRY
Discover Molecule Insights

ACTIVE PHARMA INGREDIENTS

25 API Suppliers, 9 USDMF, 8 CEP/COS, 2 EU WC, 6 KDMF, 44 NDC API, 18 Listed Suppliers, $ API Reference Price

25 API Suppliers
9 USDMF
8 CEP/COS
2 EU WC
6 KDMF
44 NDC API
18 Listed Suppliers
$ API Reference Price

DEVELOPMENTS

14 Drugs in Development

14 Drugs in Development

INTERMEDIATES

3 Intermediates Suppliers

3 Intermediates Suppliers

FINISHED DOSAGE FORMULATIONS

48 FDF Dossiers, 23 FDA Orange Book, 14 Europe, 4 Canada, 2 South Africa, 5 Listed Dossiers

48 FDF Dossiers
23 FDA Orange Book
14 Europe
4 Canada
2 South Africa
5 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CAPSULE, EXTENDED RELEASE;ORAL - 100MG;4MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, CAPSULE, EXTENDED RELEASE;ORAL - 20MG;0.8MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, CAPSULE, EXTENDED RELEASE;ORAL - 30MG;1.2MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, CAPSULE, EXTENDED RELEASE;ORAL - 50MG;2MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, CAPSULE, EXTENDED RELEASE;ORAL - 60MG;2.4MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, CAPSULE, EXTENDED RELEASE;ORAL - 80MG;3.2MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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CAPSULE, EXTENDED RELEASE;ORAL - 100MG;4MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
CAPSULE, EXTENDED RELEASE;ORAL - 20MG;0.8MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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

2 Evonik, 1 SPI Pharma, 2 Seqens, 8 DKSH, 2 Jai Radhe Sales, 4 Faran Shimi Pharmaceutical, 9 Gangwal Healthcare, 3 Nanjing Well Pharmaceutical, 1 Pfanstiehl, 4 ACG Worldwide, 8 Actylis, 1 Aeon Procare, 1 Alcedo Pharmachem, 6 Anhui Sunhere Pharmaceutical Excipients Co.,Ltd, 17 BASF, 1 Clariant, 18 Corel Pharma Chem, 6 DFE Pharma, 1 Finar, 10 Gangwal Chemicals, 9 Ideal Cures Pvt Ltd, 1 Ingredion Pharma Solutions, 35 Kerry, 4 Kima Chemical, 6 Lonza Capsugel, 11 Microlex e.U, 1 Nanjing Bold Chemical, 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, 11 Sigachi Industries, 3 The Dow Chemical Company, 1 Valens Pharmachem, 3 Vasa Pharmachem, 1 Vertellus

EXCIPIENTS BY APPLICATIONS

61 Coating Systems & Additives, 56 Fillers, Diluents & Binders, 42 Controlled & Modified Release, 25 Thickeners and Stabilizers, 24 Direct Compression, 19 Solubilizers, 19 Granulation, 15 Lubricants & Glidants, 15 Disintegrants & Superdisintegrants, 13 Co-Processed Excipients, 12 Topical, 12 Parenteral, 12 Film Formers & Plasticizers, 11 Taste Masking, 9 Empty Capsules, 7 Emulsifying Agents, 5 Rheology Modifiers, 5 API Stability Enhancers, 5 Coloring Agents, 4 Vegetarian Capsules, 4 Surfactant & Foaming Agents, 3 Chewable & Orodispersible Aids

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

DIGITAL CONTENT

47 NEWS #PharmaBuzz

47 NEWS #PharmaBuzz

GLOBAL SALES INFORMATION

2 US Medicaid Prescriptions, 17 Finished Drug Prices

2 US Medicaid Prescriptions
17 Finished Drug Prices

MARKET PLACE

16 APIs, 3 FDF Dossiers

16 APIs
3 FDF Dossiers

PATENTS & EXCLUSIVITIES

88 US Patents

88 US Patents

REF. STANDARDS & IMPURITIES

2 EDQM, 7 Others

2 EDQM
7 Others

$ API Ref.Price (USD/KG) : 6,899 Xls

Filters

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filter Applicant Reset all filters

4 All

01 1APOTEX INC

02 1BAUSCH HEALTH, CANADA INC.

03 1STERINOVA INC.

04 1TEVA CANADA LIMITED

filter Active Ingredients Reset all filters

4 All

01 4NALTREXONE HYDROCHLORIDE

filter Dosage Form Reset all filters

4 All

01 3TABLET

02 1TABLET (EXTENDED-RELEASE)

filter Brand Name Reset all filters

4 All

01 1APO-NALTREXONE

02 1CONTRAVE

03 1NALTREXONE HYDROCHLORIDE TABLETS USP

04 1REVIA

Temad Naltrexone Hydrochloride

List of Suppliers

Product Main Page

01

APOTEX INC

Pharmtech & Ingredients

Not Confirmed

APOTEX INC

Pharmtech & Ingredients

Not Confirmed

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Digital Content

Regulatory Info : Prescription

Registration Country : Canada

NALTREXONE HYDROCHLORIDE

Brand Name : APO-NALTREXONE

Dosage Form : TABLET

Dosage Strength : 50MG

Packaging : 30/50

Approval Date :

Application Number : 2444275

Regulatory Info : Prescription

Registration Country : Canada

Portfolio PDF

Product Web Link

Digital Content

Corporate PDF

02

BAUSCH HEALTH, CANADA INC.

Pharmtech & Ingredients

Not Confirmed

BAUSCH HEALTH, CANADA INC.

Pharmtech & Ingredients

Not Confirmed

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Digital Content

Regulatory Info : Prescription

Registration Country : Canada

NALTREXONE HYDROCHLORIDE

Brand Name : CONTRAVE

Dosage Form : TABLET (EXTENDED-RELEASE)

Dosage Strength : 8MG

Packaging : 70/120

Approval Date :

Application Number : 2472945

Regulatory Info : Prescription

Registration Country : Canada

Portfolio PDF

Product Web Link

Digital Content

Corporate PDF

03

STERINOVA INC.

Pharmtech & Ingredients

Not Confirmed

STERINOVA INC.

Pharmtech & Ingredients

Not Confirmed

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Digital Content

Regulatory Info : Prescription

Registration Country : Canada

NALTREXONE HYDROCHLORIDE

Brand Name : NALTREXONE HYDROCHLORIDE TABLETS USP

Dosage Form : TABLET

Dosage Strength : 50MG

Packaging : 28

Approval Date :

Application Number : 2451883

Regulatory Info : Prescription

Registration Country : Canada

Portfolio PDF

Product Web Link

Digital Content

Corporate PDF

04

TEVA CANADA LIMITED

Pharmtech & Ingredients

Not Confirmed

TEVA CANADA LIMITED

Pharmtech & Ingredients

Not Confirmed

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Digital Content

Regulatory Info : Prescription

Registration Country : Canada

NALTREXONE HYDROCHLORIDE

Brand Name : REVIA

Dosage Form : TABLET

Dosage Strength : 50MG

Packaging : 50

Approval Date :

Application Number : 2213826

Regulatory Info : Prescription

Registration Country : Canada

Portfolio PDF

Product Web Link

Digital Content

Corporate PDF

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