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 | 262.45 g/mol |
---|---|
Molecular Formula | C4H14MgO11 |
Hydrogen Bond Donor Count | 7 |
Hydrogen Bond Acceptor Count | 11 |
Rotatable Bond Count | 1 |
Exact Mass | 262.0386529 g/mol |
Monoisotopic Mass | 262.0386529 g/mol |
Topological Polar Surface Area | 126 Ų |
Heavy Atom Count | 16 |
Formal Charge | 0 |
Complexity | 123 |
Isotope Atom Count | 0 |
Defined Atom Stereocenter Count | 0 |
Undefined Atom Stereocenter Count | 2 |
Defined Bond Stereocenter Count | 0 |
Undefined Bond Stereocenter Count | 0 |
Covalently Bonded Unit Count | 7 |
ABOUT THIS PAGE
42
PharmaCompass offers a list of Magnesium Tartrate 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 Magnesium Tartrate manufacturer or Magnesium Tartrate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Magnesium Tartrate manufacturer or Magnesium Tartrate supplier.
PharmaCompass also assists you with knowing the Magnesium Tartrate API Price utilized in the formulation of products. Magnesium Tartrate API Price is not always fixed or binding as the Magnesium Tartrate Price is obtained through a variety of data sources. The Magnesium Tartrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Magnesium Tartrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Magnesium Tartrate, including repackagers and relabelers. The FDA regulates Magnesium Tartrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Magnesium Tartrate 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 Magnesium Tartrate supplier is an individual or a company that provides Magnesium Tartrate active pharmaceutical ingredient (API) or Magnesium Tartrate finished formulations upon request. The Magnesium Tartrate suppliers may include Magnesium Tartrate API manufacturers, exporters, distributors and traders.
Magnesium Tartrate 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 Magnesium Tartrate 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 Magnesium Tartrate GMP manufacturer or Magnesium Tartrate GMP API supplier for your needs.
A Magnesium Tartrate CoA (Certificate of Analysis) is a formal document that attests to Magnesium Tartrate's compliance with Magnesium Tartrate specifications and serves as a tool for batch-level quality control.
Magnesium Tartrate CoA mostly includes findings from lab analyses of a specific batch. For each Magnesium Tartrate 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.
Magnesium Tartrate may be tested according to a variety of international standards, such as European Pharmacopoeia (Magnesium Tartrate EP), Magnesium Tartrate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Magnesium Tartrate USP).