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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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1. Interferon Eicosapeptide (human Lymphoblastoid)
2. Itf-ecp
1. 79113-16-9
2. Itf-ecp
3. Interferon Eicosapeptide (human Lymphoblastoid)
4. L-glutamine, L-seryl-l-alpha-aspartyl-l-leucyl-l-prolyl-l-glutaminyl-l-threonyl-l-histidyl-l-seryl-l-leucylglycyl-l-asparaginyl-l-arginyl-l-arginyl-l-alanyl-l-leucyl-l-isoleucyl-l-leucyl-l-leucyl-l-alanyl-
Molecular Weight | 2203.5 g/mol |
---|---|
Molecular Formula | C95H163N31O29 |
XLogP3 | -9.8 |
Hydrogen Bond Donor Count | 33 |
Hydrogen Bond Acceptor Count | 33 |
Rotatable Bond Count | 75 |
Exact Mass | 2203.2266531 g/mol |
Monoisotopic Mass | 2202.2232983 g/mol |
Topological Polar Surface Area | 983 Ų |
Heavy Atom Count | 155 |
Formal Charge | 0 |
Complexity | 4930 |
Isotope Atom Count | 0 |
Defined Atom Stereocenter Count | 21 |
Undefined Atom Stereocenter Count | 1 |
Defined Bond Stereocenter Count | 0 |
Undefined Bond Stereocenter Count | 0 |
Covalently Bonded Unit Count | 1 |
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PharmaCompass offers a list of Interferon Beta-1A 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 Interferon Beta-1A manufacturer or Interferon Beta-1A supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Interferon Beta-1A manufacturer or Interferon Beta-1A supplier.
PharmaCompass also assists you with knowing the Interferon Beta-1A API Price utilized in the formulation of products. Interferon Beta-1A API Price is not always fixed or binding as the Interferon Beta-1A Price is obtained through a variety of data sources. The Interferon Beta-1A Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A interferon eicosapeptide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of interferon eicosapeptide, including repackagers and relabelers. The FDA regulates interferon eicosapeptide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. interferon eicosapeptide 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 interferon eicosapeptide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A interferon eicosapeptide supplier is an individual or a company that provides interferon eicosapeptide active pharmaceutical ingredient (API) or interferon eicosapeptide finished formulations upon request. The interferon eicosapeptide suppliers may include interferon eicosapeptide API manufacturers, exporters, distributors and traders.
click here to find a list of interferon eicosapeptide suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
interferon eicosapeptide 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 interferon eicosapeptide 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 interferon eicosapeptide GMP manufacturer or interferon eicosapeptide GMP API supplier for your needs.
A interferon eicosapeptide CoA (Certificate of Analysis) is a formal document that attests to interferon eicosapeptide's compliance with interferon eicosapeptide specifications and serves as a tool for batch-level quality control.
interferon eicosapeptide CoA mostly includes findings from lab analyses of a specific batch. For each interferon eicosapeptide 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.
interferon eicosapeptide may be tested according to a variety of international standards, such as European Pharmacopoeia (interferon eicosapeptide EP), interferon eicosapeptide JP (Japanese Pharmacopeia) and the US Pharmacopoeia (interferon eicosapeptide USP).