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
API
0
FDF
0
FDF Dossiers
0
FDA Orange Book
0
Europe
0
Canada
0
Australia
0
South Africa
0
Listed Dossiers
DRUG PRODUCT COMPOSITIONS
0
EDQM
0
USP
0
JP
0
Others
0
US Patents
0
US Exclusivities
0
Health Canada Patents
0
Data Compilation #PharmaFlow
0
Stock Recap #PipelineProspector
0
Weekly News Recap #Phispers
0
News #PharmaBuzz
US Medicaid
NA
Annual Reports
NA
Finished Drug Prices
NA
1. Gtpl9771
2. Schembl6513431
| Molecular Weight | 635.0 g/mol |
|---|---|
| Molecular Formula | C39H70O6 |
| XLogP3 | 14.1 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 6 |
| Rotatable Bond Count | 36 |
| Exact Mass | 634.51723995 g/mol |
| Monoisotopic Mass | 634.51723995 g/mol |
| Topological Polar Surface Area | 78.9 Ų |
| Heavy Atom Count | 45 |
| Formal Charge | 0 |
| Complexity | 744 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 1 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 2 |
| Covalently Bonded Unit Count | 1 |
ABOUT THIS PAGE
40
PharmaCompass offers a list of Mosedipimod 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 Mosedipimod manufacturer or Mosedipimod supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Mosedipimod manufacturer or Mosedipimod supplier.
PharmaCompass also assists you with knowing the Mosedipimod API Price utilized in the formulation of products. Mosedipimod API Price is not always fixed or binding as the Mosedipimod Price is obtained through a variety of data sources. The Mosedipimod Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Mosedipimod manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Mosedipimod, including repackagers and relabelers. The FDA regulates Mosedipimod manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Mosedipimod 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 Mosedipimod supplier is an individual or a company that provides Mosedipimod active pharmaceutical ingredient (API) or Mosedipimod finished formulations upon request. The Mosedipimod suppliers may include Mosedipimod API manufacturers, exporters, distributors and traders.
Mosedipimod 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 Mosedipimod 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 Mosedipimod GMP manufacturer or Mosedipimod GMP API supplier for your needs.
A Mosedipimod CoA (Certificate of Analysis) is a formal document that attests to Mosedipimod's compliance with Mosedipimod specifications and serves as a tool for batch-level quality control.
Mosedipimod CoA mostly includes findings from lab analyses of a specific batch. For each Mosedipimod 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.
Mosedipimod may be tested according to a variety of international standards, such as European Pharmacopoeia (Mosedipimod EP), Mosedipimod JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Mosedipimod USP).
