Synopsis
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1. Schembl15945429
| Molecular Weight | 287.29 g/mol |
|---|---|
| Molecular Formula | C14H14N4O3 |
| XLogP3 | 0 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 5 |
| Rotatable Bond Count | 1 |
| Exact Mass | g/mol |
| Monoisotopic Mass | g/mol |
| Topological Polar Surface Area | 105 |
| Heavy Atom Count | 21 |
| Formal Charge | 0 |
| Complexity | 530 |
| Isotope Atom Count | 1 |
| Defined Atom Stereocenter Count | 1 |
| 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 SP-3164 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 SP-3164 manufacturer or SP-3164 supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred SP-3164 manufacturer or SP-3164 supplier.
PharmaCompass also assists you with knowing the SP-3164 API Price utilized in the formulation of products. SP-3164 API Price is not always fixed or binding as the SP-3164 Price is obtained through a variety of data sources. The SP-3164 Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A SP-3164 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of SP-3164, including repackagers and relabelers. The FDA regulates SP-3164 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. SP-3164 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 SP-3164 supplier is an individual or a company that provides SP-3164 active pharmaceutical ingredient (API) or SP-3164 finished formulations upon request. The SP-3164 suppliers may include SP-3164 API manufacturers, exporters, distributors and traders.
SP-3164 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 SP-3164 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 SP-3164 GMP manufacturer or SP-3164 GMP API supplier for your needs.
A SP-3164 CoA (Certificate of Analysis) is a formal document that attests to SP-3164's compliance with SP-3164 specifications and serves as a tool for batch-level quality control.
SP-3164 CoA mostly includes findings from lab analyses of a specific batch. For each SP-3164 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.
SP-3164 may be tested according to a variety of international standards, such as European Pharmacopoeia (SP-3164 EP), SP-3164 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (SP-3164 USP).
