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1. Undecoylium Chloride-iodine
2. 1338-54-1
3. Unii-o4cek7fp0d
4. O4cek7fp0d
5. Undecoylium Chloride Iodine
6. Db09377
7. Undecoylium Chloride Complex With Iodine
8. Undecoylium Chloride Iodine Complex
| Molecular Weight | 272.73 g/mol |
|---|---|
| Molecular Formula | C12H17ClN2O3 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 7 |
| Exact Mass | 272.0927701 g/mol |
| Monoisotopic Mass | 272.0927701 g/mol |
| Topological Polar Surface Area | 59.3 Ų |
| Heavy Atom Count | 18 |
| Formal Charge | 0 |
| Complexity | 250 |
| 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 |
ABOUT THIS PAGE
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PharmaCompass offers a list of Emulsept 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 Emulsept manufacturer or Emulsept supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Emulsept manufacturer or Emulsept supplier.
PharmaCompass also assists you with knowing the Emulsept API Price utilized in the formulation of products. Emulsept API Price is not always fixed or binding as the Emulsept Price is obtained through a variety of data sources. The Emulsept Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A VIRAC manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of VIRAC, including repackagers and relabelers. The FDA regulates VIRAC manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. VIRAC 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 VIRAC supplier is an individual or a company that provides VIRAC active pharmaceutical ingredient (API) or VIRAC finished formulations upon request. The VIRAC suppliers may include VIRAC API manufacturers, exporters, distributors and traders.
VIRAC 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 VIRAC 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 VIRAC GMP manufacturer or VIRAC GMP API supplier for your needs.
A VIRAC CoA (Certificate of Analysis) is a formal document that attests to VIRAC's compliance with VIRAC specifications and serves as a tool for batch-level quality control.
VIRAC CoA mostly includes findings from lab analyses of a specific batch. For each VIRAC 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.
VIRAC may be tested according to a variety of international standards, such as European Pharmacopoeia (VIRAC EP), VIRAC JP (Japanese Pharmacopeia) and the US Pharmacopoeia (VIRAC USP).
