Palonosetron | Australian Register of Therapeutic Goods | Australia | PharmaCompass.com

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Palonosetron
Australia

Metrochem has been delivering customized volume & quality products to customers across the world, taking utmost care of their needs.

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EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.

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

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TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.

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Boai NKY Pharmaceuticals Ltd. is one of the largest global PVP suppliers.

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xyz-pharma-m-2025-06-09

Palonosetron

ACCESS ALL DATA, CHEMISTRY

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CHEMISTRY
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ACTIVE PHARMA INGREDIENTS

44 API Suppliers, 22 USDMF, 3 JDMF, 8 EU WC, 4 KDMF, 12 NDC API, 23 Listed Suppliers, $ API Reference Price

44 API Suppliers
22 USDMF
3 JDMF
8 EU WC
4 KDMF
12 NDC API
23 Listed Suppliers
$ API Reference Price

DEVELOPMENTS

13 Drugs in Development

13 Drugs in Development

INTERMEDIATES

11 Intermediate Suppliers

11 Intermediate Suppliers

FINISHED DOSAGE FORMULATIONS

97 FDF Dossiers, 34 FDA Orange Book, 20 Europe, 2 Canada, 10 Australia, 8 South Africa, 23 Listed Dossiers

97 FDF Dossiers
34 FDA Orange Book
20 Europe
2 Canada
10 Australia
8 South Africa
23 Listed Dossiers

DRUG PRODUCT COMPOSITIONS

CAPSULE;ORAL - 300MG;EQ 0.5MG BASE, SOLUTION;INTRAVENOUS - EQ 0.25MG BASE/5ML (EQ 0.05MG BASE/ML), POWDER;INTRAVENOUS - EQ 235MG BASE/VIAL;EQ 0.25MG BASE/VIAL, SOLUTION;INTRAVENOUS - EQ 235MG BASE/20ML (EQ 11.75MG BASE/ML);EQ 0.25MG BASE/20ML (EQ 0.0125MG BASE/ML), INJECTABLE;INTRAVENOUS - EQ 0.075MG BASE/1.5ML (EQ 0.05MG BASE/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, INJECTABLE;INTRAVENOUS - EQ 0.25MG BASE/5ML (EQ 0.05MG BASE/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, CAPSULE;ORAL - EQ 0.5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

CAPSULE;ORAL - 300MG;EQ 0.5MG BASE
SOLUTION;INTRAVENOUS - EQ 0.25MG BASE/5ML (EQ 0.05MG BASE/ML)
POWDER;INTRAVENOUS - EQ 235MG BASE/VIAL;EQ 0.25MG BASE/VIAL
SOLUTION;INTRAVENOUS - EQ 235MG BASE/20ML (EQ 11.75MG BASE/ML);EQ 0.25MG BASE/20ML (EQ 0.0125MG BASE/ML)
INJECTABLE;INTRAVENOUS - EQ 0.075MG BASE/1.5ML (EQ 0.05MG BASE/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
INJECTABLE;INTRAVENOUS - EQ 0.25MG BASE/5ML (EQ 0.05MG BASE/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
CAPSULE;ORAL - EQ 0.5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

RELATED EXCIPIENT COMPANIES

2 EUROAPI, 1 Minakem, 2 Rochem International Inc, 16 SPI Pharma, 7 DKSH, 3 Faran Shimi Pharmaceutical, 3 Boai NKY Pharmaceuticals Ltd, 6 Gangwal Healthcare, 2 Nanjing Well Pharmaceutical, 1 Shanghai Minbiotech, 1 Pfanstiehl, 4 ACG Worldwide, 6 Actylis, 5 Anhui Sunhere Pharmaceutical Excipients Co.,Ltd, 1 BASF, 3 DFE Pharma, 5 Gangwal Chemicals, 1 Ideal Cures, 2 Ingredion Pharma Solutions, 6 Kerry, 3 Lonza Capsugel, 9 Microlex e.U, 2 Pharmatrans-Sanaq, 4 Pluviaendo, 3 Prachin Chemical, 1 Qualicaps, 22 Roquette, 5 Shanghai Shenmei Pharmaceutical Technology Co., Ltd, 1 Shanghai Welltone Material Technology Co., Ltd, 2 Shijiazhuang Huaxu Pharmaceutical, 9 Sigachi Industries, 3 Silverline Chemicals, 1 Ulanqab Kema New Material, 3 Vasa Pharmachem, 1 Zhejiang Huakang Pharmaceutical

EXCIPIENTS BY APPLICATIONS

47 Fillers, Diluents & Binders, 18 Disintegrants & Superdisintegrants, 18 Direct Compression, 17 Co-Processed Excipients, 16 Lubricants & Glidants, 15 Taste Masking, 14 Chewable & Orodispersible Aids, 14 Thickeners and Stabilizers, 12 Parenteral, 11 Film Formers & Plasticizers, 10 Coating Systems & Additives, 10 Granulation, 8 Empty Capsules, 6 Controlled & Modified Release, 3 Solubilizers, 3 Emulsifying Agents, 2 API Stability Enhancers, 2 Coloring Agents, 2 Topical, 2 Rheology Modifiers, 1 Soft Gelatin

47 Fillers, Diluents & Binders
18 Disintegrants & Superdisintegrants
18 Direct Compression
17 Co-Processed Excipients
16 Lubricants & Glidants
15 Taste Masking
14 Chewable & Orodispersible Aids
14 Thickeners and Stabilizers
12 Parenteral
11 Film Formers & Plasticizers
10 Coating Systems & Additives
10 Granulation
8 Empty Capsules
6 Controlled & Modified Release
3 Solubilizers
3 Emulsifying Agents
2 API Stability Enhancers
2 Coloring Agents
2 Topical
2 Rheology Modifiers
1 Soft Gelatin

DIGITAL CONTENT

63 News #PharmaBuzz

63 News #PharmaBuzz

GLOBAL SALES INFORMATION

1 US Medicaid Prescriptions, 18 Regulatory FDF Prices, 10 Annual Reports

1 US Medicaid Prescriptions
18 Regulatory FDF Prices
10 Annual Reports

MARKET PLACE

8 APIs, 6 FDF Dossiers

8 APIs
6 FDF Dossiers

PATENTS & EXCLUSIVITIES

36 US Patents, 3 Health Canada Patents

36 US Patents
3 Health Canada Patents

REF. STANDARDS & IMPURITIES

7 Others

7 Others

$ API Ref.Price (USD/KG) : 619,282 Xls

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01 2Dr Reddy's Laboratories (Australia) Pty Ltd

02 4Juniper Biologics

03 2Juniper Biologics Pty Ltd

04 2Medsurge Healthcare Pty Ltd

filter Active Ingredients Reset all filters

10 All

01 2Fosnetupitant Chloride; Palonosetron

02 2Netupitant; Palonosetron

03 6Palonosetron

filter Dosage Form Reset all filters

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01 2Capsule

02 2Powder for Injection

03 6Blank

filter Brand Name Reset all filters

10 All

01 2Akynzeo

02 2Akynzeo IV

03 2Aloxi

04 2PALONOSETRON Medsurge

05 2Palonosetron Dr.Reddy's

List of Suppliers

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01

Juniper Biologics

DIA 2025

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Juniper Biologics

DIA 2025

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Regulatory Info :

Registration Country : Australia

Netupitant; Palonosetron

Brand Name : Akynzeo

Dosage Form : Capsule

Dosage Strength : 300MG

Packaging : 1

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Australia

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02

Juniper Biologics

DIA 2025

Not Confirmed

Juniper Biologics

DIA 2025

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Regulatory Info :

Registration Country : Australia

Netupitant; Palonosetron

Brand Name : Akynzeo

Dosage Form : Capsule

Dosage Strength : 300MG

Packaging : 1

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Australia

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03

Juniper Biologics

DIA 2025

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Juniper Biologics

DIA 2025

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Regulatory Info :

Registration Country : Australia

Fosnetupitant Chloride; Palonosetron

Brand Name : Akynzeo IV

Dosage Form : Powder for Injection

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Packaging : 1

Approval Date :

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Registration Country : Australia

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04

Juniper Biologics

DIA 2025

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Juniper Biologics

DIA 2025

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Regulatory Info :

Registration Country : Australia

Fosnetupitant Chloride; Palonosetron

Brand Name : Akynzeo IV

Dosage Form : Powder for Injection

Dosage Strength :

Packaging : 1

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Australia

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05

Juniper Biologics Pty Ltd

DIA 2025

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Juniper Biologics Pty Ltd

DIA 2025

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Registration Country : Australia

Palonosetron

Brand Name : Aloxi

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Juniper Biologics Pty Ltd

DIA 2025

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Brand Name : Aloxi

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Medsurge Healthcare Pty Ltd

DIA 2025

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Medsurge Healthcare Pty Ltd

DIA 2025

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Registration Country : Australia

Palonosetron

Brand Name : PALONOSETRON Medsurge

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Medsurge Healthcare Pty Ltd

DIA 2025

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Medsurge Healthcare Pty Ltd

DIA 2025

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Palonosetron

Brand Name : PALONOSETRON Medsurge

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Dr Reddy's Laboratories (Australia) Pty ...

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DIA 2025

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Dr Reddy's Laboratories (Australia) Pty ...

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Dr Reddy's Laboratories (Australia) Pty ...

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DIA 2025

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Dr Reddy's Laboratories (Australia) Pty ...

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DIA 2025

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Palonosetron

Brand Name : Palonosetron Dr.Reddy's

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