Synopsis
Synopsis
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USDMF
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CEP/COS
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EU WC
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KDMF
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NDC API
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VMF
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FDA Orange Book
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Canada
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Australia
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South Africa
DRUG PRODUCT COMPOSITIONS
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EDQM
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USP
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JP
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Others
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US Patents
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US Exclusivities
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Health Canada Patents
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Data Compilation #PharmaFlow
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Stock Recap #PipelineProspector
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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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ABOUT THIS PAGE
A Carbazochrome manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Carbazochrome, including repackagers and relabelers. The FDA regulates Carbazochrome manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Carbazochrome 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 Carbazochrome manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Carbazochrome supplier is an individual or a company that provides Carbazochrome active pharmaceutical ingredient (API) or Carbazochrome finished formulations upon request. The Carbazochrome suppliers may include Carbazochrome API manufacturers, exporters, distributors and traders.
click here to find a list of Carbazochrome 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 Carbazochrome Drug Master File in Japan (Carbazochrome JDMF) empowers Carbazochrome 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 Carbazochrome JDMF during the approval evaluation for pharmaceutical products. At the time of Carbazochrome 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 Carbazochrome suppliers with JDMF on PharmaCompass.
Carbazochrome 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 Carbazochrome 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 Carbazochrome GMP manufacturer or Carbazochrome GMP API supplier for your needs.
A Carbazochrome CoA (Certificate of Analysis) is a formal document that attests to Carbazochrome's compliance with Carbazochrome specifications and serves as a tool for batch-level quality control.
Carbazochrome CoA mostly includes findings from lab analyses of a specific batch. For each Carbazochrome 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.
Carbazochrome may be tested according to a variety of international standards, such as European Pharmacopoeia (Carbazochrome EP), Carbazochrome JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Carbazochrome USP).
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