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Cyclophosphamide
Canada

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

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Aurigene is a global leader in accelerating drug innovation through discovery, development & manufacturing.

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Midas Pharma provides expertise in developing and supplying APIs, finished products, and intermediates.

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ChemWerth works in generic API development & supply, non-infringement patent strategy development and regulatory support.

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

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xyz-pharma-m-2025-01-06

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Cyclophosphamide

ACCESS ALL DATA, CHEMISTRY

ACCESS ALL DATA
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CHEMISTRY
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ACTIVE PHARMA INGREDIENTS

38 API Suppliers, 21 USDMF, 6 CEP/COS, 6 EU WC, 17 NDC API, 19 Listed Suppliers, $ API Reference Price

38 API Suppliers
21 USDMF
6 CEP/COS
6 EU WC
17 NDC API
19 Listed Suppliers
$ API Reference Price

DEVELOPMENTS

314 Drugs in Development

314 Drugs in Development

INTERMEDIATES

3 Intermediates Suppliers

3 Intermediates Suppliers

FINISHED DOSAGE FORMULATIONS

139 FDF Dossiers, 79 FDA Orange Book, 15 Europe, 8 Canada, 9 Australia, 6 South Africa, 22 Listed Dossiers

139 FDF Dossiers
79 FDA Orange Book
15 Europe
8 Canada
9 Australia
6 South Africa
22 Listed Dossiers

DRUG PRODUCT COMPOSITIONS

INJECTABLE;INJECTION - 100MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, INJECTABLE;INJECTION - 1GM/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, INJECTABLE;INJECTION - 200MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, INJECTABLE;INJECTION - 2GM/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, INJECTABLE;INJECTION - 500MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, CAPSULE;ORAL - 25MG, CAPSULE;ORAL - 50MG, SOLUTION;INTRAVENOUS - 1GM/5ML (200MG/ML), SOLUTION;INTRAVENOUS - 2GM/10ML (200MG/ML), SOLUTION;INTRAVENOUS - 500MG/2.5ML (200MG/ML)

INJECTABLE;INJECTION - 100MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
INJECTABLE;INJECTION - 1GM/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
INJECTABLE;INJECTION - 200MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
INJECTABLE;INJECTION - 2GM/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
INJECTABLE;INJECTION - 500MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
CAPSULE;ORAL - 25MG
CAPSULE;ORAL - 50MG
SOLUTION;INTRAVENOUS - 1GM/5ML (200MG/ML)
SOLUTION;INTRAVENOUS - 2GM/10ML (200MG/ML)
SOLUTION;INTRAVENOUS - 500MG/2.5ML (200MG/ML)

RELATED EXCIPIENT COMPANIES

1 Minakem, 2 Rochem International Inc, 17 SPI Pharma, 7 DKSH, 4 Faran Shimi Pharmaceutical, 1 Chynops Pharma, 11 Gangwal Healthcare, 2 Nanjing Well Pharmaceutical, 1 Pfanstiehl, 4 ACG Worldwide, 1 Alcedo Pharmachem, 4 Anhui Sunhere Pharmaceutical Excipients Co.,Ltd, 2 BASF, 4 DFE Pharma, 1 Finar, 4 Gangwal Chemicals, 1 Ideal Cures Pvt Ltd, 3 Ingredion Pharma Solutions, 20 Kerry, 3 Lonza Capsugel, 11 Microlex e.U, 1 NEWEDGE Overseas, 2 Pharmatrans-Sanaq, 4 Pluviaendo, 3 Prachin Chemical, 1 Qualicaps, 17 Roquette, 2 Seppic, 4 Shanghai Shenmei Pharmaceutical Technology Co., Ltd, 1 Shijiazhuang Huaxu Pharmaceutical, 9 Sigachi Industries, 1 Valens Pharmachem, 2 Vasa Pharmachem

EXCIPIENTS BY APPLICATIONS

71 Fillers, Diluents & Binders, 32 Direct Compression, 18 Thickeners and Stabilizers, 17 Co-Processed Excipients, 16 Chewable & Orodispersible Aids, 16 Lubricants & Glidants, 14 Taste Masking, 12 Disintegrants & Superdisintegrants, 12 Granulation, 10 Coating Systems & Additives, 8 Empty Capsules, 6 Parenteral, 5 Controlled & Modified Release, 5 Film Formers & Plasticizers, 3 Coloring Agents, 3 Topical, 3 Emulsifying Agents, 2 API Stability Enhancers, 2 Solubilizers, 1 Rheology Modifiers

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

DIGITAL CONTENT

1 DATA COMPILATION #PharmaFlow, 70 NEWS #PharmaBuzz

1 DATA COMPILATION #PharmaFlow
70 NEWS #PharmaBuzz

GLOBAL SALES INFORMATION

11 Finished Drug Prices

11 Finished Drug Prices

MARKET PLACE

14 APIs, 18 FDF Dossiers

14 APIs
18 FDF Dossiers

PATENTS & EXCLUSIVITIES

12 US Patents

12 US Patents

REF. STANDARDS & IMPURITIES

1 EDQM, 5 USP, 6 Others

1 EDQM
5 USP
6 Others

$ API Ref.Price (USD/KG) : 1,060 Xls

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01 6BAXTER CORPORATION

02 2STERIMAX INC

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01 8CYCLOPHOSPHAMIDE

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01 6POWDER FOR SOLUTION

02 2TABLET

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01 2CYCLOPHOSPHAMIDE FOR INJECTION USP

02 4PROCYTOX

03 1PROCYTOX TAB 25MG

04 1PROCYTOX TAB 50MG

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01

BAXTER CORPORATION

PharmaVenue

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BAXTER CORPORATION

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Regulatory Info :

Registration Country : Canada

CYCLOPHOSPHAMIDE

Brand Name : PROCYTOX TAB 25MG

Dosage Form : TABLET

Dosage Strength : 25MG

Packaging : 200

Approval Date :

Application Number : 2241795

Regulatory Info :

Registration Country : Canada

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02

BAXTER CORPORATION

PharmaVenue

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Regulatory Info :

Registration Country : Canada

CYCLOPHOSPHAMIDE

Brand Name : PROCYTOX TAB 50MG

Dosage Form : TABLET

Dosage Strength : 50MG

Packaging : 50/100/500

Approval Date :

Application Number : 2241796

Regulatory Info :

Registration Country : Canada

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03

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Regulatory Info :

Registration Country : Canada

CYCLOPHOSPHAMIDE

Brand Name : PROCYTOX

Dosage Form : POWDER FOR SOLUTION

Dosage Strength : 200MG/VIAL

Packaging : 10ML

Approval Date :

Application Number : 2241797

Regulatory Info :

Registration Country : Canada

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04

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Regulatory Info :

Registration Country : Canada

CYCLOPHOSPHAMIDE

Brand Name : PROCYTOX

Dosage Form : POWDER FOR SOLUTION

Dosage Strength : 500MG/VIAL

Packaging : 25ML

Approval Date :

Application Number : 2241798

Regulatory Info :

Registration Country : Canada

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Regulatory Info :

Registration Country : Canada

CYCLOPHOSPHAMIDE

Brand Name : PROCYTOX

Dosage Form : POWDER FOR SOLUTION

Dosage Strength : 1000MG/VIAL

Packaging : 50ML

Approval Date :

Application Number : 2241799

Regulatory Info :

Registration Country : Canada

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Regulatory Info :

Registration Country : Canada

CYCLOPHOSPHAMIDE

Brand Name : PROCYTOX

Dosage Form : POWDER FOR SOLUTION

Dosage Strength : 2000MG/VIAL

Packaging : 100ML

Approval Date :

Application Number : 2241800

Regulatory Info :

Registration Country : Canada

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07

STERIMAX INC

PharmaVenue

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STERIMAX INC

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Regulatory Info :

Registration Country : Canada

CYCLOPHOSPHAMIDE

Brand Name : CYCLOPHOSPHAMIDE FOR INJECTION USP

Dosage Form : POWDER FOR SOLUTION

Dosage Strength : 1000MG/VIAL

Packaging :

Approval Date :

Application Number : 2547686

Regulatory Info :

Registration Country : Canada

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08

STERIMAX INC

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Regulatory Info :

Registration Country : Canada

CYCLOPHOSPHAMIDE

Brand Name : CYCLOPHOSPHAMIDE FOR INJECTION USP

Dosage Form : POWDER FOR SOLUTION

Dosage Strength : 2000MG/VIAL

Packaging :

Approval Date :

Application Number : 2547694

Regulatory Info :

Registration Country : Canada

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