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Fosaprepitant Dimeglumine
HEALTH CANADA PATENTS

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Fosaprepitant Dimeglumine

ACCESS ALL DATA, CHEMISTRY

ACCESS ALL DATA
Browse all information
CHEMISTRY
Discover Molecule Insights

ACTIVE PHARMA INGREDIENTS

35 API Suppliers, 16 USDMF, 3 JDMF, 6 EU WC, 12 NDC API, 23 Listed Suppliers, $ API Reference Price

35 API Suppliers
16 USDMF
3 JDMF
6 EU WC
12 NDC API
23 Listed Suppliers
$ API Reference Price

DEVELOPMENTS

4 Drugs in Development

4 Drugs in Development

INTERMEDIATES

3 Intermediates Suppliers

3 Intermediates Suppliers

FINISHED DOSAGE FORMULATIONS

50 FDF Dossiers, 24 FDA Orange Book, 5 Europe, 1 Canada, 8 Australia, 3 South Africa, 9 Listed Dossiers

50 FDF Dossiers
24 FDA Orange Book
5 Europe
1 Canada
8 Australia
3 South Africa
9 Listed Dossiers

DRUG PRODUCT COMPOSITIONS

POWDER;INTRAVENOUS - EQ 115MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, POWDER;INTRAVENOUS - EQ 150MG BASE/VIAL

POWDER;INTRAVENOUS - EQ 115MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
POWDER;INTRAVENOUS - EQ 150MG BASE/VIAL

RELATED EXCIPIENT COMPANIES

1 Jai Radhe Sales, 1 Nanjing Well Pharmaceutical, 3 Actylis, 1 BASF, 1 DFE Pharma, 3 Gangwal Chemicals, 7 Kerry, 1 Microlex e.U, 1 Nanjing Bold Chemical, 6 Seppic

1 Jai Radhe Sales
1 Nanjing Well Pharmaceutical
3 Actylis
1 BASF
1 DFE Pharma
3 Gangwal Chemicals
7 Kerry
1 Microlex e.U
1 Nanjing Bold Chemical
6 Seppic

EXCIPIENTS BY APPLICATIONS

10 Solubilizers, 6 Parenteral, 5 Fillers, Diluents & Binders, 3 Topical, 3 Co-Processed Excipients, 3 Direct Compression, 3 Emulsifying Agents, 2 Film Formers & Plasticizers, 2 Surfactant & Foaming Agents, 2 Thickeners and Stabilizers, 1 Granulation, 1 Rheology Modifiers, 1 API Stability Enhancers

10 Solubilizers
6 Parenteral
5 Fillers, Diluents & Binders
3 Topical
3 Co-Processed Excipients
3 Direct Compression
3 Emulsifying Agents
2 Film Formers & Plasticizers
2 Surfactant & Foaming Agents
2 Thickeners and Stabilizers
1 Granulation
1 Rheology Modifiers
1 API Stability Enhancers

DIGITAL CONTENT

31 NEWS #PharmaBuzz

31 NEWS #PharmaBuzz

GLOBAL SALES INFORMATION

3 US Medicaid Prescriptions, 3 Finished Drug Prices

3 US Medicaid Prescriptions
3 Finished Drug Prices

MARKET PLACE

1 FDF Dossiers

1 FDF Dossiers

PATENTS & EXCLUSIVITIES

2 US Patents, 2 US Exclusivities, 2 Health Canada Patents

2 US Patents
2 US Exclusivities
2 Health Canada Patents

REF. STANDARDS & IMPURITIES

2 Others

2 Others

$ API Ref.Price (USD/KG) : 20,506 Xls

Filters

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FILTER :

filter Company Reset all filters

2 All

01 1Merck Canada Inc.

02 1Merck Frosst Canada Ltd

filter Patent Reset all filters

2 All

01 22183250

filter Product Reset all filters

2 All

01 2Fosaprepitant dimeglumine

filter Dosage Reset all filters

2 All

01 1Lyophilized powder

02 1Powder for solution

filter Exp Date Reset all filters

2 All

01 22015-02-28

Chemwerth Fosaprepitant

Product Main Page

01

Merck Frosst Canada Ltd

Fosaprepitant

2024 ACI Convention

Not Confirmed

Merck Frosst Canada Ltd

2024 ACI Convention

Not Confirmed

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Patent Expiration Date : 2015-02-28

Date Granted : 2006-03-21

Fosaprepitant

Brand Name : EMEND IV

Patent Number : 2183250

Filing Date : 1995-02-28

Strength per Unit : 115 mg / vial

Dosage Form : Lyophilized powder

Human Or VET : Human

Route of Administration : Intravenous

Patent Expiration Date : 2015-02-28

Date Granted : 2006-03-21

Portfolio PDF

Product Web Link

Digital Content

Corporate PDF

02

Merck Canada Inc.

Fosaprepitant

2024 ACI Convention

Not Confirmed

Merck Canada Inc.

2024 ACI Convention

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.

Patent Expiration Date : 2015-02-28

Date Granted : 2006-03-21

Fosaprepitant

Brand Name : EMEND IV

Patent Number : 2183250

Filing Date : 1995-02-28

Strength per Unit : 150 mg

Dosage Form : Powder for solution

Human Or VET : Human

Route of Administration : Intravenous

Patent Expiration Date : 2015-02-28

Date Granted : 2006-03-21

Portfolio PDF

Product Web Link

Digital Content

Corporate PDF

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