Synopsis
Synopsis
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USDMF
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CEP/COS
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JDMF
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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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EDQM
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USP
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JP
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Others
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FDF Dossiers
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FDA Orange Book
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Europe
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Canada
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Australia
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South Africa
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Listed Dossiers
DRUG PRODUCT COMPOSITIONS
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US Patents
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US Exclusivities
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Health Canada Patents
US Medicaid
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Annual Reports
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Regulatory FDF Prices
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FDF
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Data Compilation #PharmaFlow
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Stock Recap #PipelineProspector
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Weekly News Recap #Phispers
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News #PharmaBuzz
Molecular Weight | 604.5 g/mol |
---|---|
Molecular Formula | C20H11N2Na3O10S3 |
Hydrogen Bond Donor Count | 1 |
Hydrogen Bond Acceptor Count | 12 |
Rotatable Bond Count | 2 |
Exact Mass | 603.92689092 g/mol |
Monoisotopic Mass | 603.92689092 g/mol |
Topological Polar Surface Area | 238 A^2 |
Heavy Atom Count | 38 |
Formal Charge | 0 |
Complexity | 1190 |
Isotope Atom Count | 0 |
Defined Atom Stereocenter Count | 0 |
Undefined Atom Stereocenter Count | 0 |
Defined Bond Stereocenter Count | 1 |
Undefined Bond Stereocenter Count | 0 |
Covalently Bonded Unit Count | 4 |
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ABOUT THIS PAGE
49
PharmaCompass offers a list of New Coccine 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 New Coccine manufacturer or New Coccine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred New Coccine manufacturer or New Coccine supplier.
PharmaCompass also assists you with knowing the New Coccine API Price utilized in the formulation of products. New Coccine API Price is not always fixed or binding as the New Coccine Price is obtained through a variety of data sources. The New Coccine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A New Coccin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of New Coccin, including repackagers and relabelers. The FDA regulates New Coccin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. New Coccin 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 New Coccin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A New Coccin supplier is an individual or a company that provides New Coccin active pharmaceutical ingredient (API) or New Coccin finished formulations upon request. The New Coccin suppliers may include New Coccin API manufacturers, exporters, distributors and traders.
click here to find a list of New Coccin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
New Coccin 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 New Coccin 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 New Coccin GMP manufacturer or New Coccin GMP API supplier for your needs.
A New Coccin CoA (Certificate of Analysis) is a formal document that attests to New Coccin's compliance with New Coccin specifications and serves as a tool for batch-level quality control.
New Coccin CoA mostly includes findings from lab analyses of a specific batch. For each New Coccin 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.
New Coccin may be tested according to a variety of international standards, such as European Pharmacopoeia (New Coccin EP), New Coccin JP (Japanese Pharmacopeia) and the US Pharmacopoeia (New Coccin USP).