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1. Chloride, Magnesium
2. Magnesium Chloride
3. Mgcl2
1. Magnesium Dichloride Hexahydrate
2. Bischofite
3. Polycatan
4. Magnesia Muriatica
5. Magnesium Chloride, Hexahydrate
6. Ccris 3494
7. Magnesium;dichloride;hexahydrate
8. Bischofite (mgcl2.6h2o)
9. Chlorure De Magnesium Hydrate
10. Magnesium Chloride Hydrate (mgcl2.6h2o)
11. Ins No.511
12. Chebi:86345
13. Ins-511
14. 02f3473h9o
15. E-511
16. Chlorure De Magnesium Hydrate [french]
17. Mgcl2.6h2o
18. Magnesium Chloride [usp]
19. Magnesium Chloride [ii]
20. Chembl3185229
21. Dtxsid0020789
22. Magnesium Chloride [fcc]
23. Magnesium Chloride [jan]
24. Unii-02f3473h9o
25. Magnesia Muriatica [hpus]
26. Magnesium Chloride [inci]
27. Magnesium Chloride [vandf]
28. Magnesium(ii)-chloride Hexahydrate
29. Magnesium Chloride [usp-rs]
30. Magnesium Dichloride--water (1/6)
31. Akos015855540
32. Magnesium Chloride [orange Book]
33. Ncgc00248737-01
34. Magnesium Chloride [usp Monograph]
35. Magnesium(ii) Chloride Hexahydrate
36. Magnesium Chloride Hexahydrate [mi]
37. Ft-0628076
38. Magnesium Chloride Hexahydrate A.c.s.reagent
39. Normocarb Component Magnesium Chloride
40. Magnesium Chloride Hexahydrate [who-dd]
41. Magnesium Chloride Component Of Normocarb
42. Magnesium Chloride Hexahydrate 46.5% Min Mgcl2
43. Magnesium Chloride Hexahydrate [ep Monograph]
44. Q19364448
45. 13778-96-6
Molecular Weight | 203.30 g/mol |
---|---|
Molecular Formula | Cl2H12MgO6 |
Hydrogen Bond Donor Count | 6 |
Hydrogen Bond Acceptor Count | 8 |
Rotatable Bond Count | 0 |
Exact Mass | 201.9861352 g/mol |
Monoisotopic Mass | 201.9861352 g/mol |
Topological Polar Surface Area | 6 Ų |
Heavy Atom Count | 9 |
Formal Charge | 0 |
Complexity | 0 |
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 | 9 |
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Importing Country | Total Quantity (KGS) |
Average Price (USD/KGS) |
Number of Transactions |
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REF. STANDARDS & IMPURITIES
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PharmaCompass offers a list of Magnesium Chloride 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 Magnesium Chloride manufacturer or Magnesium Chloride supplier for your needs.
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PharmaCompass also assists you with knowing the Magnesium Chloride API Price utilized in the formulation of products. Magnesium Chloride API Price is not always fixed or binding as the Magnesium Chloride Price is obtained through a variety of data sources. The Magnesium Chloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A ISOLYTE S PH 7.4 IN PLASTIC CONTAINER manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of ISOLYTE S PH 7.4 IN PLASTIC CONTAINER, including repackagers and relabelers. The FDA regulates ISOLYTE S PH 7.4 IN PLASTIC CONTAINER manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. ISOLYTE S PH 7.4 IN PLASTIC CONTAINER API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A ISOLYTE S PH 7.4 IN PLASTIC CONTAINER supplier is an individual or a company that provides ISOLYTE S PH 7.4 IN PLASTIC CONTAINER active pharmaceutical ingredient (API) or ISOLYTE S PH 7.4 IN PLASTIC CONTAINER finished formulations upon request. The ISOLYTE S PH 7.4 IN PLASTIC CONTAINER suppliers may include ISOLYTE S PH 7.4 IN PLASTIC CONTAINER API manufacturers, exporters, distributors and traders.
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A ISOLYTE S PH 7.4 IN PLASTIC CONTAINER DMF (Drug Master File) is a document detailing the whole manufacturing process of ISOLYTE S PH 7.4 IN PLASTIC CONTAINER active pharmaceutical ingredient (API) in detail. Different forms of ISOLYTE S PH 7.4 IN PLASTIC CONTAINER DMFs exist exist since differing nations have different regulations, such as ISOLYTE S PH 7.4 IN PLASTIC CONTAINER USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A ISOLYTE S PH 7.4 IN PLASTIC CONTAINER DMF submitted to regulatory agencies in the US is known as a USDMF. ISOLYTE S PH 7.4 IN PLASTIC CONTAINER USDMF includes data on ISOLYTE S PH 7.4 IN PLASTIC CONTAINER's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The ISOLYTE S PH 7.4 IN PLASTIC CONTAINER USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of ISOLYTE S PH 7.4 IN PLASTIC CONTAINER suppliers with USDMF on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The ISOLYTE S PH 7.4 IN PLASTIC CONTAINER Drug Master File in Japan (ISOLYTE S PH 7.4 IN PLASTIC CONTAINER JDMF) empowers ISOLYTE S PH 7.4 IN PLASTIC CONTAINER API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the ISOLYTE S PH 7.4 IN PLASTIC CONTAINER JDMF during the approval evaluation for pharmaceutical products. At the time of ISOLYTE S PH 7.4 IN PLASTIC CONTAINER JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a ISOLYTE S PH 7.4 IN PLASTIC CONTAINER Drug Master File in Korea (ISOLYTE S PH 7.4 IN PLASTIC CONTAINER KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of ISOLYTE S PH 7.4 IN PLASTIC CONTAINER. The MFDS reviews the ISOLYTE S PH 7.4 IN PLASTIC CONTAINER KDMF as part of the drug registration process and uses the information provided in the ISOLYTE S PH 7.4 IN PLASTIC CONTAINER KDMF to evaluate the safety and efficacy of the drug.
After submitting a ISOLYTE S PH 7.4 IN PLASTIC CONTAINER 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 ISOLYTE S PH 7.4 IN PLASTIC CONTAINER API can apply through the Korea Drug Master File (KDMF).
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A ISOLYTE S PH 7.4 IN PLASTIC CONTAINER CEP of the European Pharmacopoeia monograph is often referred to as a ISOLYTE S PH 7.4 IN PLASTIC CONTAINER Certificate of Suitability (COS). The purpose of a ISOLYTE S PH 7.4 IN PLASTIC CONTAINER CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of ISOLYTE S PH 7.4 IN PLASTIC CONTAINER EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of ISOLYTE S PH 7.4 IN PLASTIC CONTAINER to their clients by showing that a ISOLYTE S PH 7.4 IN PLASTIC CONTAINER CEP has been issued for it. The manufacturer submits a ISOLYTE S PH 7.4 IN PLASTIC CONTAINER CEP (COS) as part of the market authorization procedure, and it takes on the role of a ISOLYTE S PH 7.4 IN PLASTIC CONTAINER CEP holder for the record. Additionally, the data presented in the ISOLYTE S PH 7.4 IN PLASTIC CONTAINER CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the ISOLYTE S PH 7.4 IN PLASTIC CONTAINER DMF.
A ISOLYTE S PH 7.4 IN PLASTIC CONTAINER CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. ISOLYTE S PH 7.4 IN PLASTIC CONTAINER 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 ISOLYTE S PH 7.4 IN PLASTIC CONTAINER suppliers with CEP (COS) 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 ISOLYTE S PH 7.4 IN PLASTIC CONTAINER as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for ISOLYTE S PH 7.4 IN PLASTIC CONTAINER 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 ISOLYTE S PH 7.4 IN PLASTIC CONTAINER 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 ISOLYTE S PH 7.4 IN PLASTIC CONTAINER and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a ISOLYTE S PH 7.4 IN PLASTIC CONTAINER NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of ISOLYTE S PH 7.4 IN PLASTIC CONTAINER suppliers with NDC on PharmaCompass.
ISOLYTE S PH 7.4 IN PLASTIC CONTAINER 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 ISOLYTE S PH 7.4 IN PLASTIC CONTAINER 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 ISOLYTE S PH 7.4 IN PLASTIC CONTAINER GMP manufacturer or ISOLYTE S PH 7.4 IN PLASTIC CONTAINER GMP API supplier for your needs.
A ISOLYTE S PH 7.4 IN PLASTIC CONTAINER CoA (Certificate of Analysis) is a formal document that attests to ISOLYTE S PH 7.4 IN PLASTIC CONTAINER's compliance with ISOLYTE S PH 7.4 IN PLASTIC CONTAINER specifications and serves as a tool for batch-level quality control.
ISOLYTE S PH 7.4 IN PLASTIC CONTAINER CoA mostly includes findings from lab analyses of a specific batch. For each ISOLYTE S PH 7.4 IN PLASTIC CONTAINER 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.
ISOLYTE S PH 7.4 IN PLASTIC CONTAINER may be tested according to a variety of international standards, such as European Pharmacopoeia (ISOLYTE S PH 7.4 IN PLASTIC CONTAINER EP), ISOLYTE S PH 7.4 IN PLASTIC CONTAINER JP (Japanese Pharmacopeia) and the US Pharmacopoeia (ISOLYTE S PH 7.4 IN PLASTIC CONTAINER USP).