Synopsis
Synopsis
0
API Suppliers
0
USDMF
0
CEP/COS
0
JDMF
0
EU WC
0
KDMF
0
NDC API
0
VMF
0
Listed Suppliers
0
EDQM
0
USP
0
JP
0
Others
0
FDF Dossiers
0
FDA Orange Book
0
Europe
0
Canada
0
Australia
0
South Africa
0
Listed Dossiers
DRUG PRODUCT COMPOSITIONS
0
US Patents
0
US Exclusivities
0
Health Canada Patents
US Medicaid
NA
Annual Reports
NA
Regulatory FDF Prices
NA
0
API
0
FDF
0
Data Compilation #PharmaFlow
0
Stock Recap #PipelineProspector
0
Weekly News Recap #Phispers
0
News #PharmaBuzz
| Molecular Weight | 465.5 g/mol |
|---|---|
| Molecular Formula | C21H31N5O7 |
| XLogP3 | 2.1 |
| Hydrogen Bond Donor Count | 4 |
| Hydrogen Bond Acceptor Count | 7 |
| Rotatable Bond Count | 11 |
| Exact Mass | 465.22234834 g/mol |
| Monoisotopic Mass | 465.22234834 g/mol |
| Topological Polar Surface Area | 171 Ų |
| Heavy Atom Count | 33 |
| Formal Charge | 0 |
| Complexity | 707 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 1 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
ABOUT THIS PAGE
80
PharmaCompass offers a list of AGN-PC-071DZH 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 AGN-PC-071DZH manufacturer or AGN-PC-071DZH supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred AGN-PC-071DZH manufacturer or AGN-PC-071DZH supplier.
PharmaCompass also assists you with knowing the AGN-PC-071DZH API Price utilized in the formulation of products. AGN-PC-071DZH API Price is not always fixed or binding as the AGN-PC-071DZH Price is obtained through a variety of data sources. The AGN-PC-071DZH Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A AGN-PC-071DZH manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of AGN-PC-071DZH, including repackagers and relabelers. The FDA regulates AGN-PC-071DZH manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. AGN-PC-071DZH 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 AGN-PC-071DZH supplier is an individual or a company that provides AGN-PC-071DZH active pharmaceutical ingredient (API) or AGN-PC-071DZH finished formulations upon request. The AGN-PC-071DZH suppliers may include AGN-PC-071DZH API manufacturers, exporters, distributors and traders.
AGN-PC-071DZH 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 AGN-PC-071DZH 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 AGN-PC-071DZH GMP manufacturer or AGN-PC-071DZH GMP API supplier for your needs.
A AGN-PC-071DZH CoA (Certificate of Analysis) is a formal document that attests to AGN-PC-071DZH's compliance with AGN-PC-071DZH specifications and serves as a tool for batch-level quality control.
AGN-PC-071DZH CoA mostly includes findings from lab analyses of a specific batch. For each AGN-PC-071DZH 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.
AGN-PC-071DZH may be tested according to a variety of international standards, such as European Pharmacopoeia (AGN-PC-071DZH EP), AGN-PC-071DZH JP (Japanese Pharmacopeia) and the US Pharmacopoeia (AGN-PC-071DZH USP).
