Synopsis
Synopsis
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NDC API
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VMF
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FDA Orange Book
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Europe
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Australia
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Health Canada Patents
1. Alpha-glucoheptonic Acid
2. Alpha-glucoheptonic Acid, Calcium Salt (2:1)
3. Alpha-glucoheptonic Acid, Calcium Salt (2:1), Heptahydrate
4. Alpha-glucoheptonic Acid, Magnesium Salt (2:1)
5. Alpha-glucoheptonic Acid, Potassium Salt
6. Alpha-glucoheptonic Acid, Sodium Salt
7. Calcium Gluceptate
8. Calcium Glucoheptonate
9. Copper Glucoheptonate
10. Glucoheptonate
11. Glucoheptonic Acid
1. Calcium Glucoheptonate
2. Calcium Gluceptate
3. Calcium;(2r,3r,4s,5r,6r)-2,3,4,5,6,7-hexahydroxyheptanoate
4. A-d-glucoheptonic Acid Calcium Salt
5. Db-043867
6. Ft-0623394
7. Ft-0637507
8. Sw222262-1
9. Bis(2,3,4,5,6,7-hexahydroxyheptanoic Acid)calcium Salt
| Molecular Weight | 490.42 g/mol |
|---|---|
| Molecular Formula | C14H26CaO16 |
| Hydrogen Bond Donor Count | 12 |
| Hydrogen Bond Acceptor Count | 16 |
| Rotatable Bond Count | 10 |
| Exact Mass | 490.0846756 g/mol |
| Monoisotopic Mass | 490.0846756 g/mol |
| Topological Polar Surface Area | 323 Ų |
| Heavy Atom Count | 31 |
| Formal Charge | 0 |
| Complexity | 202 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 10 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 3 |
A - Alimentary tract and metabolism
A12 - Mineral supplements
A12A - Calcium
A12AA - Calcium
A12AA10 - Calcium glucoheptonate
API SUPPLIERS
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PharmaCompass offers a list of Calcium Glucoheptonate 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 Calcium Glucoheptonate manufacturer or Calcium Glucoheptonate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Calcium Glucoheptonate manufacturer or Calcium Glucoheptonate supplier.
PharmaCompass also assists you with knowing the Calcium Glucoheptonate API Price utilized in the formulation of products. Calcium Glucoheptonate API Price is not always fixed or binding as the Calcium Glucoheptonate Price is obtained through a variety of data sources. The Calcium Glucoheptonate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Glucoheptonate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Glucoheptonate, including repackagers and relabelers. The FDA regulates Glucoheptonate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Glucoheptonate 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 Glucoheptonate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Glucoheptonate supplier is an individual or a company that provides Glucoheptonate active pharmaceutical ingredient (API) or Glucoheptonate finished formulations upon request. The Glucoheptonate suppliers may include Glucoheptonate API manufacturers, exporters, distributors and traders.
click here to find a list of Glucoheptonate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Glucoheptonate CEP of the European Pharmacopoeia monograph is often referred to as a Glucoheptonate Certificate of Suitability (COS). The purpose of a Glucoheptonate CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Glucoheptonate EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Glucoheptonate to their clients by showing that a Glucoheptonate CEP has been issued for it. The manufacturer submits a Glucoheptonate CEP (COS) as part of the market authorization procedure, and it takes on the role of a Glucoheptonate CEP holder for the record. Additionally, the data presented in the Glucoheptonate CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Glucoheptonate DMF.
A Glucoheptonate CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Glucoheptonate CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of Glucoheptonate suppliers with CEP (COS) on PharmaCompass.
A Glucoheptonate written confirmation (Glucoheptonate WC) is an official document issued by a regulatory agency to a Glucoheptonate manufacturer, verifying that the manufacturing facility of a Glucoheptonate active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Glucoheptonate APIs or Glucoheptonate finished pharmaceutical products to another nation, regulatory agencies frequently require a Glucoheptonate WC (written confirmation) as part of the regulatory process.
click here to find a list of Glucoheptonate suppliers with Written Confirmation (WC) on PharmaCompass.
Glucoheptonate 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 Glucoheptonate 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 Glucoheptonate GMP manufacturer or Glucoheptonate GMP API supplier for your needs.
A Glucoheptonate CoA (Certificate of Analysis) is a formal document that attests to Glucoheptonate's compliance with Glucoheptonate specifications and serves as a tool for batch-level quality control.
Glucoheptonate CoA mostly includes findings from lab analyses of a specific batch. For each Glucoheptonate 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.
Glucoheptonate may be tested according to a variety of international standards, such as European Pharmacopoeia (Glucoheptonate EP), Glucoheptonate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Glucoheptonate USP).
