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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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ABOUT THIS PAGE
A Sodium Gluconate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sodium Gluconate, including repackagers and relabelers. The FDA regulates Sodium Gluconate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sodium 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 Sodium Gluconate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sodium Gluconate supplier is an individual or a company that provides Sodium Gluconate active pharmaceutical ingredient (API) or Sodium Gluconate finished formulations upon request. The Sodium Gluconate suppliers may include Sodium Gluconate API manufacturers, exporters, distributors and traders.
click here to find a list of Sodium Gluconate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Sodium Gluconate DMF (Drug Master File) is a document detailing the whole manufacturing process of Sodium Gluconate active pharmaceutical ingredient (API) in detail. Different forms of Sodium Gluconate DMFs exist exist since differing nations have different regulations, such as Sodium Gluconate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Sodium Gluconate DMF submitted to regulatory agencies in the US is known as a USDMF. Sodium Gluconate USDMF includes data on Sodium Gluconate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Sodium Gluconate USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Sodium 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 Sodium Gluconate Drug Master File in Korea (Sodium Gluconate KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Sodium Gluconate. The MFDS reviews the Sodium Gluconate KDMF as part of the drug registration process and uses the information provided in the Sodium Gluconate KDMF to evaluate the safety and efficacy of the drug.
After submitting a Sodium 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 Sodium Gluconate API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Sodium 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 Sodium Gluconate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Sodium 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 Sodium 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 Sodium Gluconate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Sodium Gluconate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Sodium Gluconate suppliers with NDC on PharmaCompass.
Sodium 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 Sodium 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 Sodium Gluconate GMP manufacturer or Sodium Gluconate GMP API supplier for your needs.
A Sodium Gluconate CoA (Certificate of Analysis) is a formal document that attests to Sodium Gluconate's compliance with Sodium Gluconate specifications and serves as a tool for batch-level quality control.
Sodium Gluconate CoA mostly includes findings from lab analyses of a specific batch. For each Sodium 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.
Sodium Gluconate may be tested according to a variety of international standards, such as European Pharmacopoeia (Sodium Gluconate EP), Sodium Gluconate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Sodium Gluconate USP).
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