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
FDF
0
Data Compilation #PharmaFlow
0
Stock Recap #PipelineProspector
0
Weekly News Recap #Phispers
0
News #PharmaBuzz
1. Eparsolfo-smit
2. Ritiometan Magnesium [who-dd]
3. Magnesium Methylidynetrithiotriacetate
4. Pbc821306w
5. Acetic Acid, 2,2',2''-(methylidynetris(thio))tris-, Magnesium Salt
6. 59672-35-4
7. Unii-pbc821306w
8. Q27286454
| Molecular Weight | 308.6 g/mol |
|---|---|
| Molecular Formula | C7H8MgO6S3 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 9 |
| Rotatable Bond Count | 7 |
| Exact Mass | 307.9333432 g/mol |
| Monoisotopic Mass | 307.9333432 g/mol |
| Topological Polar Surface Area | 194 Ų |
| Heavy Atom Count | 17 |
| Formal Charge | 0 |
| Complexity | 240 |
| 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 | 2 |
Market Place
ABOUT THIS PAGE
57
PharmaCompass offers a list of Ritiometan Magnesium 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 Ritiometan Magnesium manufacturer or Ritiometan Magnesium supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ritiometan Magnesium manufacturer or Ritiometan Magnesium supplier.
PharmaCompass also assists you with knowing the Ritiometan Magnesium API Price utilized in the formulation of products. Ritiometan Magnesium API Price is not always fixed or binding as the Ritiometan Magnesium Price is obtained through a variety of data sources. The Ritiometan Magnesium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Ritiometan Magnesium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ritiometan Magnesium, including repackagers and relabelers. The FDA regulates Ritiometan Magnesium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ritiometan Magnesium 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 Ritiometan Magnesium supplier is an individual or a company that provides Ritiometan Magnesium active pharmaceutical ingredient (API) or Ritiometan Magnesium finished formulations upon request. The Ritiometan Magnesium suppliers may include Ritiometan Magnesium API manufacturers, exporters, distributors and traders.
Ritiometan Magnesium 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 Ritiometan Magnesium 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 Ritiometan Magnesium GMP manufacturer or Ritiometan Magnesium GMP API supplier for your needs.
A Ritiometan Magnesium CoA (Certificate of Analysis) is a formal document that attests to Ritiometan Magnesium's compliance with Ritiometan Magnesium specifications and serves as a tool for batch-level quality control.
Ritiometan Magnesium CoA mostly includes findings from lab analyses of a specific batch. For each Ritiometan Magnesium 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.
Ritiometan Magnesium may be tested according to a variety of international standards, such as European Pharmacopoeia (Ritiometan Magnesium EP), Ritiometan Magnesium JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Ritiometan Magnesium USP).
