Synopsis
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USDMF
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NDC API
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1. 10402-15-0
2. Copper;2-hydroxypropane-1,2,3-tricarboxylic Acid
3. Caswell No. 235b
4. Citric Acid, Copper Salt
5. Chelates Of Copper Citrate
6. Epa Pesticide Chemical Code 044005
7. 5153-00-4
Molecular Weight | 255.67 g/mol |
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Molecular Formula | C6H8CuO7+2 |
Hydrogen Bond Donor Count | 4 |
Hydrogen Bond Acceptor Count | 7 |
Rotatable Bond Count | 5 |
Exact Mass | 254.956600 g/mol |
Monoisotopic Mass | 254.956600 g/mol |
Topological Polar Surface Area | 132 Ų |
Heavy Atom Count | 14 |
Formal Charge | 2 |
Complexity | 227 |
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 Imports and Exports
Importing Country | Total Quantity (KGS) |
Average Price (USD/KGS) |
Number of Transactions |
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ABOUT THIS PAGE
A Copper Citrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Copper Citrate, including repackagers and relabelers. The FDA regulates Copper Citrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Copper Citrate 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 Copper Citrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Copper Citrate supplier is an individual or a company that provides Copper Citrate active pharmaceutical ingredient (API) or Copper Citrate finished formulations upon request. The Copper Citrate suppliers may include Copper Citrate API manufacturers, exporters, distributors and traders.
click here to find a list of Copper Citrate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
Copper Citrate 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 Copper Citrate 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 Copper Citrate GMP manufacturer or Copper Citrate GMP API supplier for your needs.
A Copper Citrate CoA (Certificate of Analysis) is a formal document that attests to Copper Citrate's compliance with Copper Citrate specifications and serves as a tool for batch-level quality control.
Copper Citrate CoA mostly includes findings from lab analyses of a specific batch. For each Copper Citrate 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.
Copper Citrate may be tested according to a variety of international standards, such as European Pharmacopoeia (Copper Citrate EP), Copper Citrate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Copper Citrate USP).
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