Synopsis
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1. Schembl535500
| Molecular Weight | 159.14 g/mol |
|---|---|
| Molecular Formula | C8H8NaO2 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 2 |
| Exact Mass | 159.04219878 g/mol |
| Monoisotopic Mass | 159.04219878 g/mol |
| Topological Polar Surface Area | 26.3 Ų |
| Heavy Atom Count | 11 |
| Formal Charge | 0 |
| Complexity | 114 |
| 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 |
API SUPPLIERS
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API Imports and Exports
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ABOUT THIS PAGE
A Sodium Phenyl Acetate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sodium Phenyl Acetate, including repackagers and relabelers. The FDA regulates Sodium Phenyl Acetate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sodium Phenyl Acetate 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 Sodium Phenyl Acetate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sodium Phenyl Acetate supplier is an individual or a company that provides Sodium Phenyl Acetate active pharmaceutical ingredient (API) or Sodium Phenyl Acetate finished formulations upon request. The Sodium Phenyl Acetate suppliers may include Sodium Phenyl Acetate API manufacturers, exporters, distributors and traders.
click here to find a list of Sodium Phenyl Acetate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Sodium Phenyl Acetate written confirmation (Sodium Phenyl Acetate WC) is an official document issued by a regulatory agency to a Sodium Phenyl Acetate manufacturer, verifying that the manufacturing facility of a Sodium Phenyl Acetate active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Sodium Phenyl Acetate APIs or Sodium Phenyl Acetate finished pharmaceutical products to another nation, regulatory agencies frequently require a Sodium Phenyl Acetate WC (written confirmation) as part of the regulatory process.
click here to find a list of Sodium Phenyl Acetate suppliers with Written Confirmation (WC) on PharmaCompass.
Sodium Phenyl Acetate 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 Sodium Phenyl Acetate 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 Sodium Phenyl Acetate GMP manufacturer or Sodium Phenyl Acetate GMP API supplier for your needs.
A Sodium Phenyl Acetate CoA (Certificate of Analysis) is a formal document that attests to Sodium Phenyl Acetate's compliance with Sodium Phenyl Acetate specifications and serves as a tool for batch-level quality control.
Sodium Phenyl Acetate CoA mostly includes findings from lab analyses of a specific batch. For each Sodium Phenyl Acetate 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.
Sodium Phenyl Acetate may be tested according to a variety of international standards, such as European Pharmacopoeia (Sodium Phenyl Acetate EP), Sodium Phenyl Acetate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Sodium Phenyl Acetate USP).
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