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1. Insulin, Single Chain Des-(b30)-
2. Sci Des-(b30)
1. Sci Des-(b30)
2. Insulin, Single Chain Des-(b30)-
3. Insulin (ox), 8a-l-threonine-10a-l-isoleucine-30b-de-l-alanine-
4. 39416-73-4
Molecular Weight | 5706 g/mol |
---|---|
Molecular Formula | C253H376N64O75S6 |
XLogP3 | -12.2 |
Hydrogen Bond Donor Count | 76 |
Hydrogen Bond Acceptor Count | 87 |
Rotatable Bond Count | 176 |
Exact Mass | 5704.5966814 g/mol |
Monoisotopic Mass | 5702.5899718 g/mol |
Topological Polar Surface Area | 2400 Ų |
Heavy Atom Count | 398 |
Formal Charge | 0 |
Complexity | 14300 |
Isotope Atom Count | 0 |
Defined Atom Stereocenter Count | 50 |
Undefined Atom Stereocenter Count | 0 |
Defined Bond Stereocenter Count | 0 |
Undefined Bond Stereocenter Count | 0 |
Covalently Bonded Unit Count | 1 |
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PharmaCompass offers a list of Insulin Dalanted 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 Insulin Dalanted manufacturer or Insulin Dalanted supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Insulin Dalanted manufacturer or Insulin Dalanted supplier.
PharmaCompass also assists you with knowing the Insulin Dalanted API Price utilized in the formulation of products. Insulin Dalanted API Price is not always fixed or binding as the Insulin Dalanted Price is obtained through a variety of data sources. The Insulin Dalanted Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A ILETIN I manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of ILETIN I, including repackagers and relabelers. The FDA regulates ILETIN I manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. ILETIN I API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A ILETIN I supplier is an individual or a company that provides ILETIN I active pharmaceutical ingredient (API) or ILETIN I finished formulations upon request. The ILETIN I suppliers may include ILETIN I API manufacturers, exporters, distributors and traders.
ILETIN I 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 ILETIN I 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 ILETIN I GMP manufacturer or ILETIN I GMP API supplier for your needs.
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ILETIN I CoA mostly includes findings from lab analyses of a specific batch. For each ILETIN I 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.
ILETIN I may be tested according to a variety of international standards, such as European Pharmacopoeia (ILETIN I EP), ILETIN I JP (Japanese Pharmacopeia) and the US Pharmacopoeia (ILETIN I USP).