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1. Sorbitan Trioleate (inn/nf)
2. D05898
| Molecular Weight | 957.5 g/mol |
|---|---|
| Molecular Formula | C60H108O8 |
| XLogP3 | 21.5 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 8 |
| Rotatable Bond Count | 53 |
| Exact Mass | 956.80442040 g/mol |
| Monoisotopic Mass | 956.80442040 g/mol |
| Topological Polar Surface Area | 108 Ų |
| Heavy Atom Count | 68 |
| Formal Charge | 0 |
| Complexity | 1230 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 3 |
| Undefined Atom Stereocenter Count | 1 |
| Defined Bond Stereocenter Count | 3 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
ABOUT THIS PAGE
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PharmaCompass offers a list of D05898 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 D05898 manufacturer or D05898 supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred D05898 manufacturer or D05898 supplier.
PharmaCompass also assists you with knowing the D05898 API Price utilized in the formulation of products. D05898 API Price is not always fixed or binding as the D05898 Price is obtained through a variety of data sources. The D05898 Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A D05898 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of D05898, including repackagers and relabelers. The FDA regulates D05898 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. D05898 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 D05898 supplier is an individual or a company that provides D05898 active pharmaceutical ingredient (API) or D05898 finished formulations upon request. The D05898 suppliers may include D05898 API manufacturers, exporters, distributors and traders.
D05898 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 D05898 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 D05898 GMP manufacturer or D05898 GMP API supplier for your needs.
A D05898 CoA (Certificate of Analysis) is a formal document that attests to D05898's compliance with D05898 specifications and serves as a tool for batch-level quality control.
D05898 CoA mostly includes findings from lab analyses of a specific batch. For each D05898 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.
D05898 may be tested according to a variety of international standards, such as European Pharmacopoeia (D05898 EP), D05898 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (D05898 USP).
