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| Molecular Weight | 459.5 g/mol |
|---|---|
| Molecular Formula | C20H25N7O6 |
| XLogP3 | -0.5 |
| Hydrogen Bond Donor Count | 7 |
| Hydrogen Bond Acceptor Count | 9 |
| Rotatable Bond Count | 9 |
| Exact Mass | 459.18663154 g/mol |
| Monoisotopic Mass | 459.18663154 g/mol |
| Topological Polar Surface Area | 199 A^2 |
| Heavy Atom Count | 33 |
| Formal Charge | 0 |
| Complexity | 865 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 2 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
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ABOUT THIS PAGE
A Levomefolate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Levomefolate, including repackagers and relabelers. The FDA regulates Levomefolate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Levomefolate API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Levomefolate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Levomefolate supplier is an individual or a company that provides Levomefolate active pharmaceutical ingredient (API) or Levomefolate finished formulations upon request. The Levomefolate suppliers may include Levomefolate API manufacturers, exporters, distributors and traders.
click here to find a list of Levomefolate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
Levomefolate 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 Levomefolate 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 Levomefolate GMP manufacturer or Levomefolate GMP API supplier for your needs.
A Levomefolate CoA (Certificate of Analysis) is a formal document that attests to Levomefolate's compliance with Levomefolate specifications and serves as a tool for batch-level quality control.
Levomefolate CoA mostly includes findings from lab analyses of a specific batch. For each Levomefolate 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.
Levomefolate may be tested according to a variety of international standards, such as European Pharmacopoeia (Levomefolate EP), Levomefolate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Levomefolate USP).
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