Close
4

Athena Athena

X

Find Treosulfan manufacturers, exporters & distributors on PharmaCompass

PharmaCompass
API SUPPLIERS
API Suppliers

API Suppliers

US DMFs Filed

US DMFs Filed

CEP/COS Certifications

CEP/COS Certifications

0

JDMFs Filed

JDMFs Filed

0

Other Certificates

Other Certificates

Other Suppliers

Other Suppliers

API REF. PRICE (USD / KG)

0

INTERMEDIATES

0

DOSSIERS // FDF
USA (Orange Book)

USA (Orange Book)

0

Europe

Europe

0

Canada

Canada

Australia

Australia

0

South Africa

South Africa

0

Uploaded Dossiers

Uploaded Dossiers

GLOBAL SALES (USD Million)

U.S. Medicaid

0

Annual Reports

0

EXCIPIENTS

0

PATENTS & EXCLUSIVITIES

USFDA Orange Book Patents

0

USFDA Exclusivities

0

DIGITAL CONTENT

Blog #PharmaFlow

0

News

REF STANDARD

EDQM

0

USP

0

JP

0

Other Listed Suppliers

0

SERVICES

0

Looking for 299-75-2 / Treosulfan API manufacturers, exporters & distributors?

Treosulfan manufacturers, exporters & distributors 1

70

PharmaCompass offers a list of Treosulfan API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Treosulfan manufacturer or Treosulfan supplier for your needs.

Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Treosulfan manufacturer or Treosulfan supplier.

PharmaCompass also assists you with knowing the Treosulfan API Price utilized in the formulation of products. Treosulfan API Price is not always fixed or binding as the Treosulfan Price is obtained through a variety of data sources. The Treosulfan Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.

API | Excipient name

Treosulfan

Synonyms

299-75-2, Treosulphan, Ovastat, Threosulphan, Dihydroxybusulfan, Nsc 39069

Cas Number

299-75-2

Unique Ingredient Identifier (UNII)

CO61ER3EPI

About Treosulfan

Treosulfan is the prodrug of a bifunctional sulfonate alkylating agent with myeloablative, immunosuppressive, and antineoplastic activities. Under physiological conditions, treosulfan converts nonenzymatically to L-diepoxybutane via a monoepoxide intermediate. The monoepoxide intermediate and L-diepoxybutane alkylate DNA at guanine residues and produce DNA interstrand crosslinks, resulting in DNA fragmentation and apoptosis. In escalated doses, this agent also exhibits myeloablative and immunosuppressive activities.

Treosulfan Manufacturers

A Treosulfan manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Treosulfan, including repackagers and relabelers. The FDA regulates Treosulfan manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Treosulfan API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.

click here to find a list of Treosulfan manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

Treosulfan Suppliers

A Treosulfan supplier is an individual or a company that provides Treosulfan active pharmaceutical ingredient (API) or Treosulfan finished formulations upon request. The Treosulfan suppliers may include Treosulfan API manufacturers, exporters, distributors and traders.

click here to find a list of Treosulfan suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

Treosulfan USDMF

A Treosulfan DMF (Drug Master File) is a document detailing the whole manufacturing process of Treosulfan active pharmaceutical ingredient (API) in detail. Different forms of Treosulfan DMFs exist exist since differing nations have different regulations, such as Treosulfan USDMF, ASMF (EDMF), JDMF, CDMF, etc.

A Treosulfan DMF submitted to regulatory agencies in the US is known as a USDMF. Treosulfan USDMF includes data on Treosulfan's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Treosulfan USDMF is kept confidential to protect the manufacturer’s intellectual property.

click here to find a list of Treosulfan suppliers with USDMF on PharmaCompass.

Treosulfan WC

A Treosulfan written confirmation (Treosulfan WC) is an official document issued by a regulatory agency to a Treosulfan manufacturer, verifying that the manufacturing facility of a Treosulfan active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Treosulfan APIs or Treosulfan finished pharmaceutical products to another nation, regulatory agencies frequently require a Treosulfan WC (written confirmation) as part of the regulatory process.

click here to find a list of Treosulfan suppliers with Written Confirmation (WC) on PharmaCompass.

Treosulfan GMP

Treosulfan Active pharmaceutical ingredient (API) is produced in GMP-certified manufacturing facility.

GMP stands for Good Manufacturing Practices, which is a system used in the pharmaceutical industry to make sure that goods are regularly produced and monitored in accordance with quality standards. The FDA’s current Good Manufacturing Practices requirements are referred to as cGMP or current GMP which indicates that the company follows the most recent GMP specifications. The World Health Organization (WHO) has its own set of GMP guidelines, called the WHO GMP. Different countries can also set their own guidelines for GMP like China (Chinese GMP) or the EU (EU GMP).

PharmaCompass offers a list of Treosulfan GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, API price, and more, enabling you to easily find the right Treosulfan GMP manufacturer or Treosulfan GMP API supplier for your needs.

Treosulfan CoA

A Treosulfan CoA (Certificate of Analysis) is a formal document that attests to Treosulfan's compliance with Treosulfan specifications and serves as a tool for batch-level quality control.

Treosulfan CoA mostly includes findings from lab analyses of a specific batch. For each Treosulfan CoA document that a company creates, the USFDA specifies specific requirements, such as supplier information, material identification, transportation data, evidence of conformity and signature data.

Treosulfan may be tested according to a variety of international standards, such as European Pharmacopoeia (Treosulfan EP), Treosulfan JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Treosulfan USP).

Inform the supplier about your product requirements, specifying if you need a product with particular monograph like EP (Ph. Eur.), USP, JP, BP, or any other quality. In addition, clarify whether you need hydrochloride (HCl), anhydricum, base, micronisatum or a specific level of purity. To find reputable suppliers, utilize the filters and select those certified by GMP, FDA, or any other certification as per your requirement.
For your convenience, we have listed synonyms and CAS numbers to help you find the best supplier. The use of synonyms and CAS numbers can be helpful in identifying potential suppliers, but it is crucial to note that they might not always indicate the exact same product. It is important to confirm the product details with the supplier before making a purchase to ensure that it meets your requirements.
Ask Us for Pharmaceutical Supplier and Partner
Ask Us, Find A Supplier / Partner
No Commissions, No Strings Attached, Get Connected for FREE

What are you looking for?

How can we help you?

The request can't be empty

Please read our Privacy Policy carefully

You must agree to the privacy policy

The name can't be empty
The company can't be empty.
The email can't be empty Please enter a valid email.
The mobile can't be empty
Post Enquiry
POST ENQUIRY