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1. 5-ketoproline
2. 5-oxoproline
3. 5-oxopyrrolidine-2-carboxylic Acid
4. Pidolate, Magnesium
5. Pidolic Acid
6. Pyroglutamate
7. Pyroglutamic Acid
8. Pyrrolidonecarboxylic Acid
1. Magnesium Pyroglutamate
2. 62003-27-4
3. Magnesium Pca
4. Pidolic Acid Magnesium Salt (2:1)
5. V5pc588n7g
6. 135701-98-3
7. L-proline, 5-oxo-, Magnesium Salt (2:1)
8. Magnesium;(2s)-5-oxopyrrolidine-2-carboxylate
9. Unii-v5pc588n7g
10. Mag2
11. Einecs 263-365-7
12. 5-oxo-l-proline Magnesium Salt (2:1)
13. Bis(5-oxo-l-prolinato-n1,o2)magnesium
14. Magnesium Pca [inci]
15. Schembl7928170
16. Chembl3707303
17. Magnesium Pidolate [mart.]
18. Magnesium Pidolate [who-dd]
19. Db13301
20. Magnesium Pidolate [ep Monograph]
21. Q27291565
22. Magnesium, Bis(5-oxo-l-prolinato-n1,o2)-, (t-4)-
| Molecular Weight | 280.52 g/mol |
|---|---|
| Molecular Formula | C10H12MgN2O6 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 6 |
| Rotatable Bond Count | 0 |
| Exact Mass | 280.0545778 g/mol |
| Monoisotopic Mass | 280.0545778 g/mol |
| Topological Polar Surface Area | 139 Ų |
| Heavy Atom Count | 19 |
| Formal Charge | 0 |
| Complexity | 149 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 2 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 3 |
A - Alimentary tract and metabolism
A12 - Mineral supplements
A12C - Other mineral supplements
A12CC - Magnesium
A12CC08 - Magnesium pidolate
API SUPPLIERS
Certificate Number : R1-CEP 2008-224 - Rev 02
Issue Date : 2019-08-05
Type : Chemical
Substance Number : 1619
Status : Valid
Certificate Number : R1-CEP 2016-064 - Rev 01
Issue Date : 2023-08-29
Type : Chemical
Substance Number : 1619
Status : Valid
Date of Issue : 2022-06-08
Valid Till : 2025-07-07
Written Confirmation Number : WC-0104
Address of the Firm :
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CEP/COS
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API Imports and Exports
| Importing Country | Total Quantity (KGS) |
Average Price (USD/KGS) |
Number of Transactions |
|---|
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REF. STANDARDS & IMPURITIES
ABOUT THIS PAGE
A Magnesium Pidolate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Magnesium Pidolate, including repackagers and relabelers. The FDA regulates Magnesium Pidolate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Magnesium Pidolate 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 Magnesium Pidolate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Magnesium Pidolate supplier is an individual or a company that provides Magnesium Pidolate active pharmaceutical ingredient (API) or Magnesium Pidolate finished formulations upon request. The Magnesium Pidolate suppliers may include Magnesium Pidolate API manufacturers, exporters, distributors and traders.
click here to find a list of Magnesium Pidolate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Magnesium Pidolate CEP of the European Pharmacopoeia monograph is often referred to as a Magnesium Pidolate Certificate of Suitability (COS). The purpose of a Magnesium Pidolate CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Magnesium Pidolate EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Magnesium Pidolate to their clients by showing that a Magnesium Pidolate CEP has been issued for it. The manufacturer submits a Magnesium Pidolate CEP (COS) as part of the market authorization procedure, and it takes on the role of a Magnesium Pidolate CEP holder for the record. Additionally, the data presented in the Magnesium Pidolate CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Magnesium Pidolate DMF.
A Magnesium Pidolate CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Magnesium Pidolate 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 Magnesium Pidolate suppliers with CEP (COS) on PharmaCompass.
A Magnesium Pidolate written confirmation (Magnesium Pidolate WC) is an official document issued by a regulatory agency to a Magnesium Pidolate manufacturer, verifying that the manufacturing facility of a Magnesium Pidolate active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Magnesium Pidolate APIs or Magnesium Pidolate finished pharmaceutical products to another nation, regulatory agencies frequently require a Magnesium Pidolate WC (written confirmation) as part of the regulatory process.
click here to find a list of Magnesium Pidolate suppliers with Written Confirmation (WC) on PharmaCompass.
Magnesium Pidolate 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 Magnesium Pidolate 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 Magnesium Pidolate GMP manufacturer or Magnesium Pidolate GMP API supplier for your needs.
A Magnesium Pidolate CoA (Certificate of Analysis) is a formal document that attests to Magnesium Pidolate's compliance with Magnesium Pidolate specifications and serves as a tool for batch-level quality control.
Magnesium Pidolate CoA mostly includes findings from lab analyses of a specific batch. For each Magnesium Pidolate 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.
Magnesium Pidolate may be tested according to a variety of international standards, such as European Pharmacopoeia (Magnesium Pidolate EP), Magnesium Pidolate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Magnesium Pidolate USP).
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