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| Molecular Weight | 373.4 g/mol |
|---|---|
| Molecular Formula | C21H15N3O4 |
| XLogP3 | 3.8 |
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 7 |
| Rotatable Bond Count | 2 |
| Exact Mass | 373.10625597 g/mol |
| Monoisotopic Mass | 373.10625597 g/mol |
| Topological Polar Surface Area | 98.7 A^2 |
| Heavy Atom Count | 28 |
| Formal Charge | 0 |
| Complexity | 912 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 2 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
| 1 of 2 | |
|---|---|
| Drug Name | Exjade |
| PubMed Health | Deferasirox (By mouth) |
| Drug Classes | Heavy Metal Chelator |
| Drug Label | Exjade(deferasirox) is an iron chelating agent. Exjade tablets for oral suspension contain 125mg, 250mg, or 500mg deferasirox. Deferasirox is designated chemically as 4-[3,5-Bis (2-hydroxyphenyl)-1H-1,2,4-triazol-1-yl]-benzoic acid and its st... |
| Active Ingredient | Deferasirox |
| Dosage Form | Tablet, for suspension |
| Route | Oral |
| Strength | 250mg; 125mg; 500mg |
| Market Status | Prescription |
| Company | Novartis |
| 2 of 2 | |
|---|---|
| Drug Name | Exjade |
| PubMed Health | Deferasirox (By mouth) |
| Drug Classes | Heavy Metal Chelator |
| Drug Label | Exjade(deferasirox) is an iron chelating agent. Exjade tablets for oral suspension contain 125mg, 250mg, or 500mg deferasirox. Deferasirox is designated chemically as 4-[3,5-Bis (2-hydroxyphenyl)-1H-1,2,4-triazol-1-yl]-benzoic acid and its st... |
| Active Ingredient | Deferasirox |
| Dosage Form | Tablet, for suspension |
| Route | Oral |
| Strength | 250mg; 125mg; 500mg |
| Market Status | Prescription |
| Company | Novartis |
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DOSAGE - GRANULE;ORAL - 180MG
USFDA APPLICATION NUMBER - 207968
DOSAGE - GRANULE;ORAL - 360MG
USFDA APPLICATION NUMBER - 207968
DOSAGE - GRANULE;ORAL - 90MG
USFDA APPLICATION NUMBER - 207968
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PharmaCompass offers a list of Deferasirox 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 Deferasirox manufacturer or Deferasirox supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Deferasirox manufacturer or Deferasirox supplier.
PharmaCompass also assists you with knowing the Deferasirox API Price utilized in the formulation of products. Deferasirox API Price is not always fixed or binding as the Deferasirox Price is obtained through a variety of data sources. The Deferasirox Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Exjade manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Exjade, including repackagers and relabelers. The FDA regulates Exjade manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Exjade 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 Exjade manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Exjade supplier is an individual or a company that provides Exjade active pharmaceutical ingredient (API) or Exjade finished formulations upon request. The Exjade suppliers may include Exjade API manufacturers, exporters, distributors and traders.
click here to find a list of Exjade suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Exjade DMF (Drug Master File) is a document detailing the whole manufacturing process of Exjade active pharmaceutical ingredient (API) in detail. Different forms of Exjade DMFs exist exist since differing nations have different regulations, such as Exjade USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Exjade DMF submitted to regulatory agencies in the US is known as a USDMF. Exjade USDMF includes data on Exjade's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Exjade USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Exjade suppliers with USDMF on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Exjade Drug Master File in Japan (Exjade JDMF) empowers Exjade API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Exjade JDMF during the approval evaluation for pharmaceutical products. At the time of Exjade JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Exjade suppliers with JDMF 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 Exjade Drug Master File in Korea (Exjade KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Exjade. The MFDS reviews the Exjade KDMF as part of the drug registration process and uses the information provided in the Exjade KDMF to evaluate the safety and efficacy of the drug.
After submitting a Exjade 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 Exjade API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Exjade suppliers with KDMF on PharmaCompass.
A Exjade CEP of the European Pharmacopoeia monograph is often referred to as a Exjade Certificate of Suitability (COS). The purpose of a Exjade CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Exjade EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Exjade to their clients by showing that a Exjade CEP has been issued for it. The manufacturer submits a Exjade CEP (COS) as part of the market authorization procedure, and it takes on the role of a Exjade CEP holder for the record. Additionally, the data presented in the Exjade CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Exjade DMF.
A Exjade CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Exjade CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of Exjade suppliers with CEP (COS) on PharmaCompass.
A Exjade written confirmation (Exjade WC) is an official document issued by a regulatory agency to a Exjade manufacturer, verifying that the manufacturing facility of a Exjade active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Exjade APIs or Exjade finished pharmaceutical products to another nation, regulatory agencies frequently require a Exjade WC (written confirmation) as part of the regulatory process.
click here to find a list of Exjade 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 Exjade as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Exjade 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 Exjade 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 Exjade and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Exjade NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Exjade suppliers with NDC on PharmaCompass.
Exjade 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 Exjade 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 Exjade GMP manufacturer or Exjade GMP API supplier for your needs.
A Exjade CoA (Certificate of Analysis) is a formal document that attests to Exjade's compliance with Exjade specifications and serves as a tool for batch-level quality control.
Exjade CoA mostly includes findings from lab analyses of a specific batch. For each Exjade 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.
Exjade may be tested according to a variety of international standards, such as European Pharmacopoeia (Exjade EP), Exjade JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Exjade USP).
