Close
4

Athena Athena

X

Find Axitinib 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)
INTERMEDIATES
DOSSIERS // FDF
USA (Orange Book)

USA (Orange Book)

Europe

Europe

Canada

Canada

Australia

Australia

South Africa

South Africa

Uploaded Dossiers

Uploaded Dossiers

GLOBAL SALES (USD Million)

U.S. Medicaid

Annual Reports

EXCIPIENTS
PATENTS & EXCLUSIVITIES

USFDA Orange Book Patents

USFDA Exclusivities

0

DIGITAL CONTENT

Blog #PharmaFlow

News

REF STANDARD

EDQM

0

USP

0

JP

0

Other Listed Suppliers

SERVICES

0

Looking for 319460-85-0 / Axitinib API manufacturers, exporters & distributors?

Axitinib manufacturers, exporters & distributors 1

53

PharmaCompass offers a list of Axitinib 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 Axitinib manufacturer or Axitinib supplier for your needs.

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

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

API | Excipient name

Axitinib

Synonyms

319460-85-0, Ag-013736, Inlyta, Ag 013736, (e)-n-methyl-2-((3-(2-(pyridin-2-yl)vinyl)-1h-indazol-6-yl)thio)benzamide, Ag-13736

Cas Number

319460-85-0

Unique Ingredient Identifier (UNII)

C9LVQ0YUXG

About Axitinib

A benzamide and indazole derivative that acts as a TYROSINE KINASE inhibitor of the VASCULAR ENDOTHELIAL GROWTH FACTOR RECEPTOR. It is used in the treatment of advanced RENAL CELL CARCINOMA.

DSSTox_CID_28975 Manufacturers

A DSSTox_CID_28975 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DSSTox_CID_28975, including repackagers and relabelers. The FDA regulates DSSTox_CID_28975 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DSSTox_CID_28975 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 DSSTox_CID_28975 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

DSSTox_CID_28975 Suppliers

A DSSTox_CID_28975 supplier is an individual or a company that provides DSSTox_CID_28975 active pharmaceutical ingredient (API) or DSSTox_CID_28975 finished formulations upon request. The DSSTox_CID_28975 suppliers may include DSSTox_CID_28975 API manufacturers, exporters, distributors and traders.

click here to find a list of DSSTox_CID_28975 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

DSSTox_CID_28975 USDMF

A DSSTox_CID_28975 DMF (Drug Master File) is a document detailing the whole manufacturing process of DSSTox_CID_28975 active pharmaceutical ingredient (API) in detail. Different forms of DSSTox_CID_28975 DMFs exist exist since differing nations have different regulations, such as DSSTox_CID_28975 USDMF, ASMF (EDMF), JDMF, CDMF, etc.

A DSSTox_CID_28975 DMF submitted to regulatory agencies in the US is known as a USDMF. DSSTox_CID_28975 USDMF includes data on DSSTox_CID_28975's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The DSSTox_CID_28975 USDMF is kept confidential to protect the manufacturer’s intellectual property.

click here to find a list of DSSTox_CID_28975 suppliers with USDMF on PharmaCompass.

DSSTox_CID_28975 KDMF

In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.

Pharmaceutical companies submit a DSSTox_CID_28975 Drug Master File in Korea (DSSTox_CID_28975 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of DSSTox_CID_28975. The MFDS reviews the DSSTox_CID_28975 KDMF as part of the drug registration process and uses the information provided in the DSSTox_CID_28975 KDMF to evaluate the safety and efficacy of the drug.

After submitting a DSSTox_CID_28975 KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their DSSTox_CID_28975 API can apply through the Korea Drug Master File (KDMF).

click here to find a list of DSSTox_CID_28975 suppliers with KDMF on PharmaCompass.

DSSTox_CID_28975 WC

A DSSTox_CID_28975 written confirmation (DSSTox_CID_28975 WC) is an official document issued by a regulatory agency to a DSSTox_CID_28975 manufacturer, verifying that the manufacturing facility of a DSSTox_CID_28975 active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting DSSTox_CID_28975 APIs or DSSTox_CID_28975 finished pharmaceutical products to another nation, regulatory agencies frequently require a DSSTox_CID_28975 WC (written confirmation) as part of the regulatory process.

click here to find a list of DSSTox_CID_28975 suppliers with Written Confirmation (WC) on PharmaCompass.

DSSTox_CID_28975 NDC

National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing DSSTox_CID_28975 as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for DSSTox_CID_28975 API and other APIs are published in this directory by the FDA.

Unfinished drugs

The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.

Pharmaceutical companies that manufacture DSSTox_CID_28975 as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.

Compounded drug products

The NDC directory also contains data on finished compounded human drug products that contain DSSTox_CID_28975 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a DSSTox_CID_28975 NDC to their finished compounded human drug products, they may choose to do so.

click here to find a list of DSSTox_CID_28975 suppliers with NDC on PharmaCompass.

DSSTox_CID_28975 GMP

DSSTox_CID_28975 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 DSSTox_CID_28975 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 DSSTox_CID_28975 GMP manufacturer or DSSTox_CID_28975 GMP API supplier for your needs.

DSSTox_CID_28975 CoA

A DSSTox_CID_28975 CoA (Certificate of Analysis) is a formal document that attests to DSSTox_CID_28975's compliance with DSSTox_CID_28975 specifications and serves as a tool for batch-level quality control.

DSSTox_CID_28975 CoA mostly includes findings from lab analyses of a specific batch. For each DSSTox_CID_28975 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.

DSSTox_CID_28975 may be tested according to a variety of international standards, such as European Pharmacopoeia (DSSTox_CID_28975 EP), DSSTox_CID_28975 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (DSSTox_CID_28975 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