Synopsis
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NDC API
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Data Compilation #PharmaFlow
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| Molecular Weight | 364.4 g/mol |
|---|---|
| Molecular Formula | C20H20N4O3 |
| XLogP3 | 2.3 |
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 2 |
| Exact Mass | 364.15354051 g/mol |
| Monoisotopic Mass | 364.15354051 g/mol |
| Topological Polar Surface Area | 86.6 A^2 |
| Heavy Atom Count | 27 |
| Formal Charge | 0 |
| Complexity | 767 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 1 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
Drugs in Development
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PharmaCompass offers a list of ADX-1612 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 ADX-1612 manufacturer or ADX-1612 supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred ADX-1612 manufacturer or ADX-1612 supplier.
PharmaCompass also assists you with knowing the ADX-1612 API Price utilized in the formulation of products. ADX-1612 API Price is not always fixed or binding as the ADX-1612 Price is obtained through a variety of data sources. The ADX-1612 Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A ADX-1612 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of ADX-1612, including repackagers and relabelers. The FDA regulates ADX-1612 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. ADX-1612 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 ADX-1612 supplier is an individual or a company that provides ADX-1612 active pharmaceutical ingredient (API) or ADX-1612 finished formulations upon request. The ADX-1612 suppliers may include ADX-1612 API manufacturers, exporters, distributors and traders.
ADX-1612 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 ADX-1612 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 ADX-1612 GMP manufacturer or ADX-1612 GMP API supplier for your needs.
A ADX-1612 CoA (Certificate of Analysis) is a formal document that attests to ADX-1612's compliance with ADX-1612 specifications and serves as a tool for batch-level quality control.
ADX-1612 CoA mostly includes findings from lab analyses of a specific batch. For each ADX-1612 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.
ADX-1612 may be tested according to a variety of international standards, such as European Pharmacopoeia (ADX-1612 EP), ADX-1612 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (ADX-1612 USP).
