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JP
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Molecular Weight | 236.23 g/mol |
---|---|
Molecular Formula | C10H12N4O3 |
XLogP3 | -1.6 |
Hydrogen Bond Donor Count | 3 |
Hydrogen Bond Acceptor Count | 5 |
Rotatable Bond Count | 1 |
Exact Mass | 236.09094026 g/mol |
Monoisotopic Mass | 236.09094026 g/mol |
Topological Polar Surface Area | 108 A^2 |
Heavy Atom Count | 17 |
Formal Charge | 0 |
Complexity | 478 |
Isotope Atom Count | 0 |
Defined Atom Stereocenter Count | 0 |
Undefined Atom Stereocenter Count | 1 |
Defined Bond Stereocenter Count | 1 |
Undefined Bond Stereocenter Count | 0 |
Covalently Bonded Unit Count | 1 |
API Imports and Exports
Importing Country | Total Quantity (KGS) |
Average Price (USD/KGS) |
Number of Transactions |
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PharmaCompass offers a list of Carbazochrome 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 Carbazochrome manufacturer or Carbazochrome supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Carbazochrome manufacturer or Carbazochrome supplier.
PharmaCompass also assists you with knowing the Carbazochrome API Price utilized in the formulation of products. Carbazochrome API Price is not always fixed or binding as the Carbazochrome Price is obtained through a variety of data sources. The Carbazochrome Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Adrenochrome monosemicarbazon manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Adrenochrome monosemicarbazon, including repackagers and relabelers. The FDA regulates Adrenochrome monosemicarbazon manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Adrenochrome monosemicarbazon 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 Adrenochrome monosemicarbazon manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Adrenochrome monosemicarbazon supplier is an individual or a company that provides Adrenochrome monosemicarbazon active pharmaceutical ingredient (API) or Adrenochrome monosemicarbazon finished formulations upon request. The Adrenochrome monosemicarbazon suppliers may include Adrenochrome monosemicarbazon API manufacturers, exporters, distributors and traders.
click here to find a list of Adrenochrome monosemicarbazon suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information 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 Adrenochrome monosemicarbazon Drug Master File in Japan (Adrenochrome monosemicarbazon JDMF) empowers Adrenochrome monosemicarbazon 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 Adrenochrome monosemicarbazon JDMF during the approval evaluation for pharmaceutical products. At the time of Adrenochrome monosemicarbazon 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 Adrenochrome monosemicarbazon suppliers with JDMF on PharmaCompass.
Adrenochrome monosemicarbazon 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 Adrenochrome monosemicarbazon 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 Adrenochrome monosemicarbazon GMP manufacturer or Adrenochrome monosemicarbazon GMP API supplier for your needs.
A Adrenochrome monosemicarbazon CoA (Certificate of Analysis) is a formal document that attests to Adrenochrome monosemicarbazon's compliance with Adrenochrome monosemicarbazon specifications and serves as a tool for batch-level quality control.
Adrenochrome monosemicarbazon CoA mostly includes findings from lab analyses of a specific batch. For each Adrenochrome monosemicarbazon 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.
Adrenochrome monosemicarbazon may be tested according to a variety of international standards, such as European Pharmacopoeia (Adrenochrome monosemicarbazon EP), Adrenochrome monosemicarbazon JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Adrenochrome monosemicarbazon USP).