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API SUPPLIERS
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USDMF
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Tagoor's product development expertise, backed by our comprehensive understanding of the processes, helps us offer high-quality APIs.
4-Chloro-6,7-dimethoxyquinoline
CAS Number : 35654-56-9
End Use API : Cabozantinib
About The Company : Tagoor Laboratories, established in 2018, is a part of the Tagoor Group. It specializes in providing APIs, advanced intermediates and key starting materials for...
Tagoor's product development expertise, backed by our comprehensive understanding of the processes, helps us offer high-quality APIs.
1-((4-Fluoro phenyl) Carbamoyl) Cyclopropane Carbo...
CAS Number : 849217-48-7
End Use API : Cabozantinib
About The Company : Tagoor Laboratories, established in 2018, is a part of the Tagoor Group. It specializes in providing APIs, advanced intermediates and key starting materials for...
Tagoor's product development expertise, backed by our comprehensive understanding of the processes, helps us offer high-quality APIs.
4-((6,7-Dimethoxyquinolin-4-yl)oxy)aniline
CAS Number : 190728-25-7
End Use API : Cabozantinib
About The Company : Tagoor Laboratories, established in 2018, is a part of the Tagoor Group. It specializes in providing APIs, advanced intermediates and key starting materials for...
Tagoor's product development expertise, backed by our comprehensive understanding of the processes, helps us offer high-quality APIs.
Cyclopropane-1,1-dicarboxylic acid methyl ester
CAS Number : 113020-21-6
End Use API : Cabozantinib
About The Company : Tagoor Laboratories, established in 2018, is a part of the Tagoor Group. It specializes in providing APIs, advanced intermediates and key starting materials for...
Tagoor's product development expertise, backed by our comprehensive understanding of the processes, helps us offer high-quality APIs.
1,1-Cyclopropanedicarboxylic acid
CAS Number : 598-10-7
End Use API : Cabozantinib
About The Company : Tagoor Laboratories, established in 2018, is a part of the Tagoor Group. It specializes in providing APIs, advanced intermediates and key starting materials for...
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DOSAGE - CAPSULE;ORAL - EQ 20MG BASE
USFDA APPLICATION NUMBER - 203756
DOSAGE - CAPSULE;ORAL - EQ 80MG BASE
USFDA APPLICATION NUMBER - 203756
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REF. STANDARDS & IMPURITIES
ABOUT THIS PAGE
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PharmaCompass offers a list of Cabozantinib 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 Cabozantinib manufacturer or Cabozantinib supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Cabozantinib manufacturer or Cabozantinib supplier.
PharmaCompass also assists you with knowing the Cabozantinib API Price utilized in the formulation of products. Cabozantinib API Price is not always fixed or binding as the Cabozantinib Price is obtained through a variety of data sources. The Cabozantinib Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Cabozantinib L-Malate Salt manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cabozantinib L-Malate Salt, including repackagers and relabelers. The FDA regulates Cabozantinib L-Malate Salt manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cabozantinib L-Malate Salt 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 Cabozantinib L-Malate Salt manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cabozantinib L-Malate Salt supplier is an individual or a company that provides Cabozantinib L-Malate Salt active pharmaceutical ingredient (API) or Cabozantinib L-Malate Salt finished formulations upon request. The Cabozantinib L-Malate Salt suppliers may include Cabozantinib L-Malate Salt API manufacturers, exporters, distributors and traders.
click here to find a list of Cabozantinib L-Malate Salt suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Cabozantinib L-Malate Salt DMF (Drug Master File) is a document detailing the whole manufacturing process of Cabozantinib L-Malate Salt active pharmaceutical ingredient (API) in detail. Different forms of Cabozantinib L-Malate Salt DMFs exist exist since differing nations have different regulations, such as Cabozantinib L-Malate Salt USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Cabozantinib L-Malate Salt DMF submitted to regulatory agencies in the US is known as a USDMF. Cabozantinib L-Malate Salt USDMF includes data on Cabozantinib L-Malate Salt's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Cabozantinib L-Malate Salt USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Cabozantinib L-Malate Salt suppliers with USDMF on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Cabozantinib L-Malate Salt Drug Master File in Korea (Cabozantinib L-Malate Salt KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Cabozantinib L-Malate Salt. The MFDS reviews the Cabozantinib L-Malate Salt KDMF as part of the drug registration process and uses the information provided in the Cabozantinib L-Malate Salt KDMF to evaluate the safety and efficacy of the drug.
After submitting a Cabozantinib L-Malate Salt 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 Cabozantinib L-Malate Salt API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Cabozantinib L-Malate Salt suppliers with KDMF on PharmaCompass.
A Cabozantinib L-Malate Salt written confirmation (Cabozantinib L-Malate Salt WC) is an official document issued by a regulatory agency to a Cabozantinib L-Malate Salt manufacturer, verifying that the manufacturing facility of a Cabozantinib L-Malate Salt active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Cabozantinib L-Malate Salt APIs or Cabozantinib L-Malate Salt finished pharmaceutical products to another nation, regulatory agencies frequently require a Cabozantinib L-Malate Salt WC (written confirmation) as part of the regulatory process.
click here to find a list of Cabozantinib L-Malate Salt suppliers with Written Confirmation (WC) on PharmaCompass.
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 Cabozantinib L-Malate Salt as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Cabozantinib L-Malate Salt API and other APIs are published in this directory by the FDA.
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 Cabozantinib L-Malate Salt 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.
The NDC directory also contains data on finished compounded human drug products that contain Cabozantinib L-Malate Salt and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Cabozantinib L-Malate Salt NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Cabozantinib L-Malate Salt suppliers with NDC on PharmaCompass.
Cabozantinib L-Malate Salt 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 Cabozantinib L-Malate Salt 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 Cabozantinib L-Malate Salt GMP manufacturer or Cabozantinib L-Malate Salt GMP API supplier for your needs.
A Cabozantinib L-Malate Salt CoA (Certificate of Analysis) is a formal document that attests to Cabozantinib L-Malate Salt's compliance with Cabozantinib L-Malate Salt specifications and serves as a tool for batch-level quality control.
Cabozantinib L-Malate Salt CoA mostly includes findings from lab analyses of a specific batch. For each Cabozantinib L-Malate Salt 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.
Cabozantinib L-Malate Salt may be tested according to a variety of international standards, such as European Pharmacopoeia (Cabozantinib L-Malate Salt EP), Cabozantinib L-Malate Salt JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Cabozantinib L-Malate Salt USP).
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