Synopsis
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1. Schembl16998942
| Molecular Weight | 402.5 g/mol |
|---|---|
| Molecular Formula | C21H30N4O4 |
| XLogP3 | 3.7 |
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 6 |
| Rotatable Bond Count | 5 |
| Exact Mass | 402.22670545 g/mol |
| Monoisotopic Mass | 402.22670545 g/mol |
| Topological Polar Surface Area | 126 Ų |
| Heavy Atom Count | 29 |
| Formal Charge | 0 |
| Complexity | 606 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 3 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
ABOUT THIS PAGE
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PharmaCompass offers a list of EP-7041 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 EP-7041 manufacturer or EP-7041 supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred EP-7041 manufacturer or EP-7041 supplier.
PharmaCompass also assists you with knowing the EP-7041 API Price utilized in the formulation of products. EP-7041 API Price is not always fixed or binding as the EP-7041 Price is obtained through a variety of data sources. The EP-7041 Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A EP-7041 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of EP-7041, including repackagers and relabelers. The FDA regulates EP-7041 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. EP-7041 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 EP-7041 supplier is an individual or a company that provides EP-7041 active pharmaceutical ingredient (API) or EP-7041 finished formulations upon request. The EP-7041 suppliers may include EP-7041 API manufacturers, exporters, distributors and traders.
EP-7041 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 EP-7041 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 EP-7041 GMP manufacturer or EP-7041 GMP API supplier for your needs.
A EP-7041 CoA (Certificate of Analysis) is a formal document that attests to EP-7041's compliance with EP-7041 specifications and serves as a tool for batch-level quality control.
EP-7041 CoA mostly includes findings from lab analyses of a specific batch. For each EP-7041 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.
EP-7041 may be tested according to a variety of international standards, such as European Pharmacopoeia (EP-7041 EP), EP-7041 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (EP-7041 USP).
