Synopsis
Synopsis
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API Suppliers
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USDMF
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CEP/COS
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EU WC
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KDMF
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NDC API
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VMF
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EDQM
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USP
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JP
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FDF Dossiers
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FDA Orange Book
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Europe
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Australia
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South Africa
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Listed Dossiers
DRUG PRODUCT COMPOSITIONS
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US Exclusivities
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Health Canada Patents
US Medicaid
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| Molecular Weight | 355.4 g/mol |
|---|---|
| Molecular Formula | C18H18FN5O2 |
| XLogP3 | 1.4 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 5 |
| Rotatable Bond Count | 0 |
| Exact Mass | 355.14445300 g/mol |
| Monoisotopic Mass | 355.14445300 g/mol |
| Topological Polar Surface Area | 78.3 A^2 |
| Heavy Atom Count | 26 |
| Formal Charge | 0 |
| Complexity | 716 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 2 |
| 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 TPX-0005 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 TPX-0005 manufacturer or TPX-0005 supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred TPX-0005 manufacturer or TPX-0005 supplier.
PharmaCompass also assists you with knowing the TPX-0005 API Price utilized in the formulation of products. TPX-0005 API Price is not always fixed or binding as the TPX-0005 Price is obtained through a variety of data sources. The TPX-0005 Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A TPX-0005 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of TPX-0005, including repackagers and relabelers. The FDA regulates TPX-0005 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. TPX-0005 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 TPX-0005 supplier is an individual or a company that provides TPX-0005 active pharmaceutical ingredient (API) or TPX-0005 finished formulations upon request. The TPX-0005 suppliers may include TPX-0005 API manufacturers, exporters, distributors and traders.
TPX-0005 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 TPX-0005 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 TPX-0005 GMP manufacturer or TPX-0005 GMP API supplier for your needs.
A TPX-0005 CoA (Certificate of Analysis) is a formal document that attests to TPX-0005's compliance with TPX-0005 specifications and serves as a tool for batch-level quality control.
TPX-0005 CoA mostly includes findings from lab analyses of a specific batch. For each TPX-0005 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.
TPX-0005 may be tested according to a variety of international standards, such as European Pharmacopoeia (TPX-0005 EP), TPX-0005 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (TPX-0005 USP).
