Synopsis
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1. Chembl363443
| Molecular Weight | 341.4 g/mol |
|---|---|
| Molecular Formula | C19H19NO5 |
| XLogP3 | 3.4 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 5 |
| Rotatable Bond Count | 5 |
| Exact Mass | 341.12632271 g/mol |
| Monoisotopic Mass | 341.12632271 g/mol |
| Topological Polar Surface Area | 58.9 Ų |
| Heavy Atom Count | 25 |
| Formal Charge | 0 |
| Complexity | 445 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| 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 Agn-Pc-004Wxe 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-004Wxe manufacturer or Agn-Pc-004Wxe supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Agn-Pc-004Wxe manufacturer or Agn-Pc-004Wxe supplier.
PharmaCompass also assists you with knowing the Agn-Pc-004Wxe API Price utilized in the formulation of products. Agn-Pc-004Wxe API Price is not always fixed or binding as the Agn-Pc-004Wxe Price is obtained through a variety of data sources. The Agn-Pc-004Wxe Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Agn-Pc-004Wxe manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Agn-Pc-004Wxe, including repackagers and relabelers. The FDA regulates Agn-Pc-004Wxe manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Agn-Pc-004Wxe 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-004Wxe supplier is an individual or a company that provides Agn-Pc-004Wxe active pharmaceutical ingredient (API) or Agn-Pc-004Wxe finished formulations upon request. The Agn-Pc-004Wxe suppliers may include Agn-Pc-004Wxe API manufacturers, exporters, distributors and traders.
click here to find a list of Agn-Pc-004Wxe suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Agn-Pc-004Wxe DMF (Drug Master File) is a document detailing the whole manufacturing process of Agn-Pc-004Wxe active pharmaceutical ingredient (API) in detail. Different forms of Agn-Pc-004Wxe DMFs exist exist since differing nations have different regulations, such as Agn-Pc-004Wxe USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Agn-Pc-004Wxe DMF submitted to regulatory agencies in the US is known as a USDMF. Agn-Pc-004Wxe USDMF includes data on Agn-Pc-004Wxe's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Agn-Pc-004Wxe USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Agn-Pc-004Wxe suppliers with USDMF on PharmaCompass.
Agn-Pc-004Wxe 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-004Wxe 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-004Wxe GMP manufacturer or Agn-Pc-004Wxe GMP API supplier for your needs.
A Agn-Pc-004Wxe CoA (Certificate of Analysis) is a formal document that attests to Agn-Pc-004Wxe's compliance with Agn-Pc-004Wxe specifications and serves as a tool for batch-level quality control.
Agn-Pc-004Wxe CoA mostly includes findings from lab analyses of a specific batch. For each Agn-Pc-004Wxe 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-004Wxe may be tested according to a variety of international standards, such as European Pharmacopoeia (Agn-Pc-004Wxe EP), Agn-Pc-004Wxe JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Agn-Pc-004Wxe USP).
