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1. Ginger Rhizome
2. Ginger Root
3. Rhizoma Zingiberis
4. Rhizoma Zingiberis Recens
5. Zingiberis Rhizoma
6. Zingiberis Rhizoma Praeparatum
7. Zingiberis Siccatum Rhizoma
1. 84696-15-1
2. (e)-1-(4-hydroxy-3-methoxyphenyl)dec-4-en-3-one;1-(4-hydroxy-3-methoxyphenyl)-5-methyldecan-3-one
Molecular Weight | 568.8 g/mol |
---|---|
Molecular Formula | C35H52O6 |
Hydrogen Bond Donor Count | 2 |
Hydrogen Bond Acceptor Count | 6 |
Rotatable Bond Count | 19 |
Exact Mass | 568.37638937 g/mol |
Monoisotopic Mass | 568.37638937 g/mol |
Topological Polar Surface Area | 93.1 Ų |
Heavy Atom Count | 41 |
Formal Charge | 0 |
Complexity | 589 |
Isotope Atom Count | 0 |
Defined Atom Stereocenter Count | 0 |
Undefined Atom Stereocenter Count | 1 |
Defined Bond Stereocenter Count | 1 |
Undefined Bond Stereocenter Count | 0 |
Covalently Bonded Unit Count | 2 |
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PharmaCompass offers a list of Ginger extract 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 Ginger extract manufacturer or Ginger extract supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ginger extract manufacturer or Ginger extract supplier.
PharmaCompass also assists you with knowing the Ginger extract API Price utilized in the formulation of products. Ginger extract API Price is not always fixed or binding as the Ginger extract Price is obtained through a variety of data sources. The Ginger extract Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A EINECS 283-634-2 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of EINECS 283-634-2, including repackagers and relabelers. The FDA regulates EINECS 283-634-2 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. EINECS 283-634-2 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 EINECS 283-634-2 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A EINECS 283-634-2 supplier is an individual or a company that provides EINECS 283-634-2 active pharmaceutical ingredient (API) or EINECS 283-634-2 finished formulations upon request. The EINECS 283-634-2 suppliers may include EINECS 283-634-2 API manufacturers, exporters, distributors and traders.
click here to find a list of EINECS 283-634-2 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
EINECS 283-634-2 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 EINECS 283-634-2 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 EINECS 283-634-2 GMP manufacturer or EINECS 283-634-2 GMP API supplier for your needs.
A EINECS 283-634-2 CoA (Certificate of Analysis) is a formal document that attests to EINECS 283-634-2's compliance with EINECS 283-634-2 specifications and serves as a tool for batch-level quality control.
EINECS 283-634-2 CoA mostly includes findings from lab analyses of a specific batch. For each EINECS 283-634-2 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.
EINECS 283-634-2 may be tested according to a variety of international standards, such as European Pharmacopoeia (EINECS 283-634-2 EP), EINECS 283-634-2 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (EINECS 283-634-2 USP).