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1. Boron Gluconate
2. D-gluconate
3. D-gluconic Acid
4. Dextronic Acid
5. Gluconate
6. Gluconic Acid
7. Gluconic Acid, (113)indium-labeled
8. Gluconic Acid, (14)c-labeled
9. Gluconic Acid, (159)dysprosium-labeled Salt
10. Gluconic Acid, (99)technecium (5+) Salt
11. Gluconic Acid, 1-(14)c-labeled
12. Gluconic Acid, 6-(14)c-labeled
13. Gluconic Acid, Aluminum (3:1) Salt
14. Gluconic Acid, Ammonium Salt
15. Gluconic Acid, Calcium Salt
16. Gluconic Acid, Cesium(+3) Salt
17. Gluconic Acid, Cobalt (2:1) Salt
18. Gluconic Acid, Copper Salt
19. Gluconic Acid, Fe(+2) Salt, Dihydrate
20. Gluconic Acid, Lanthanum(+3) Salt
21. Gluconic Acid, Magnesium (2:1) Salt
22. Gluconic Acid, Manganese (2:1) Salt
23. Gluconic Acid, Monolithium Salt
24. Gluconic Acid, Monopotassium Salt
25. Gluconic Acid, Monosodium Salt
26. Gluconic Acid, Potassium Salt
27. Gluconic Acid, Strontium (2:1) Salt
28. Gluconic Acid, Tin(+2) Salt
29. Gluconic Acid, Zinc Salt
30. Lithium Gluconate
31. Magnerot
32. Magnesium Gluconate
33. Maltonic Acid
34. Manganese Gluconate
35. Pentahydroxycaproic Acid
36. Sodium Gluconate
37. Zinc Gluconate
1. Sodium Galactonate
2. D-gluconic Acid Sodium Salt;sodium D-gluconate;d-gluconate Sodium Salt
3. Schembl23641
4. Bcp13391
5. Akos026749890
6. Sb45452
7. Sodium Gluconate 45% (technical Grade)
8. Ft-0626723
9. Gluconate Sodium;d-gluconic Acid Sodium Salt; Sodium D-gluconate; D-gluconate Sodium Salt
| Molecular Weight | 218.14 g/mol |
|---|---|
| Molecular Formula | C6H11NaO7 |
| Hydrogen Bond Donor Count | 5 |
| Hydrogen Bond Acceptor Count | 7 |
| Rotatable Bond Count | 5 |
| Exact Mass | 218.04024697 g/mol |
| Monoisotopic Mass | 218.04024697 g/mol |
| Topological Polar Surface Area | 141 Ų |
| Heavy Atom Count | 14 |
| Formal Charge | 0 |
| Complexity | 176 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 4 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 2 |
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Evonik
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ABOUT THIS PAGE
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PharmaCompass offers a list of Sodium Gluconate 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 Sodium Gluconate manufacturer or Sodium Gluconate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Sodium Gluconate manufacturer or Sodium Gluconate supplier.
PharmaCompass also assists you with knowing the Sodium Gluconate API Price utilized in the formulation of products. Sodium Gluconate API Price is not always fixed or binding as the Sodium Gluconate Price is obtained through a variety of data sources. The Sodium Gluconate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Monosodium gluconate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Monosodium gluconate, including repackagers and relabelers. The FDA regulates Monosodium gluconate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Monosodium gluconate 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 Monosodium gluconate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Monosodium gluconate supplier is an individual or a company that provides Monosodium gluconate active pharmaceutical ingredient (API) or Monosodium gluconate finished formulations upon request. The Monosodium gluconate suppliers may include Monosodium gluconate API manufacturers, exporters, distributors and traders.
click here to find a list of Monosodium gluconate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Monosodium gluconate DMF (Drug Master File) is a document detailing the whole manufacturing process of Monosodium gluconate active pharmaceutical ingredient (API) in detail. Different forms of Monosodium gluconate DMFs exist exist since differing nations have different regulations, such as Monosodium gluconate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Monosodium gluconate DMF submitted to regulatory agencies in the US is known as a USDMF. Monosodium gluconate USDMF includes data on Monosodium gluconate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Monosodium gluconate USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Monosodium gluconate suppliers with USDMF on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Monosodium gluconate Drug Master File in Korea (Monosodium gluconate KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Monosodium gluconate. The MFDS reviews the Monosodium gluconate KDMF as part of the drug registration process and uses the information provided in the Monosodium gluconate KDMF to evaluate the safety and efficacy of the drug.
After submitting a Monosodium gluconate KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their Monosodium gluconate API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Monosodium gluconate suppliers with KDMF on PharmaCompass.
National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Monosodium gluconate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Monosodium gluconate API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture Monosodium gluconate as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain Monosodium gluconate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Monosodium gluconate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Monosodium gluconate suppliers with NDC on PharmaCompass.
Monosodium gluconate 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 Monosodium gluconate 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 Monosodium gluconate GMP manufacturer or Monosodium gluconate GMP API supplier for your needs.
A Monosodium gluconate CoA (Certificate of Analysis) is a formal document that attests to Monosodium gluconate's compliance with Monosodium gluconate specifications and serves as a tool for batch-level quality control.
Monosodium gluconate CoA mostly includes findings from lab analyses of a specific batch. For each Monosodium gluconate 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.
Monosodium gluconate may be tested according to a variety of international standards, such as European Pharmacopoeia (Monosodium gluconate EP), Monosodium gluconate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Monosodium gluconate USP).
