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1. 1317-26-6
2. Aluminum Hydroxide/magnesium Hydroxide
3. Aluminum Hydroxide/magnesium Hydroxide - Magaldrate C410
4. Aluminum Hydroxide/magnesium Hydroxide - Magaldrate C632
| Molecular Weight | 86.310 g/mol |
|---|---|
| Molecular Formula | AlH3MgO2- |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 0 |
| Exact Mass | 85.9798844 g/mol |
| Monoisotopic Mass | 85.9798844 g/mol |
| Topological Polar Surface Area | 2 Ų |
| Heavy Atom Count | 4 |
| Formal Charge | -1 |
| 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 | 4 |
A02AD02
S76 | LUXPHARMA | Pharmaceuticals Marketed in Luxembourg | Pharmaceuticals marketed in Luxembourg, as published by d'Gesondheetskeess (CNS, la caisse nationale de sante, www.cns.lu), mapped by name to structures using CompTox by R. Singh et al. (in prep.). List downloaded from https://cns.public.lu/en/legislations/textes-coordonnes/liste-med-comm.html. Dataset DOI:10.5281/zenodo.4587355
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PharmaCompass offers a list of Magaldrate 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 Magaldrate manufacturer or Magaldrate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Magaldrate manufacturer or Magaldrate supplier.
PharmaCompass also assists you with knowing the Magaldrate API Price utilized in the formulation of products. Magaldrate API Price is not always fixed or binding as the Magaldrate Price is obtained through a variety of data sources. The Magaldrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Eurim brand of magaldrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Eurim brand of magaldrate, including repackagers and relabelers. The FDA regulates Eurim brand of magaldrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Eurim brand of magaldrate 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 Eurim brand of magaldrate supplier is an individual or a company that provides Eurim brand of magaldrate active pharmaceutical ingredient (API) or Eurim brand of magaldrate finished formulations upon request. The Eurim brand of magaldrate suppliers may include Eurim brand of magaldrate API manufacturers, exporters, distributors and traders.
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A Eurim brand of magaldrate DMF (Drug Master File) is a document detailing the whole manufacturing process of Eurim brand of magaldrate active pharmaceutical ingredient (API) in detail. Different forms of Eurim brand of magaldrate DMFs exist exist since differing nations have different regulations, such as Eurim brand of magaldrate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Eurim brand of magaldrate DMF submitted to regulatory agencies in the US is known as a USDMF. Eurim brand of magaldrate USDMF includes data on Eurim brand of magaldrate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Eurim brand of magaldrate USDMF is kept confidential to protect the manufacturer’s intellectual property.
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A Eurim brand of magaldrate written confirmation (Eurim brand of magaldrate WC) is an official document issued by a regulatory agency to a Eurim brand of magaldrate manufacturer, verifying that the manufacturing facility of a Eurim brand of magaldrate active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Eurim brand of magaldrate APIs or Eurim brand of magaldrate finished pharmaceutical products to another nation, regulatory agencies frequently require a Eurim brand of magaldrate WC (written confirmation) as part of the regulatory process.
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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 Eurim brand of magaldrate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Eurim brand of magaldrate 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 Eurim brand of magaldrate 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 Eurim brand of magaldrate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Eurim brand of magaldrate NDC to their finished compounded human drug products, they may choose to do so.
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Eurim brand of magaldrate 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 Eurim brand of magaldrate 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 Eurim brand of magaldrate GMP manufacturer or Eurim brand of magaldrate GMP API supplier for your needs.
A Eurim brand of magaldrate CoA (Certificate of Analysis) is a formal document that attests to Eurim brand of magaldrate's compliance with Eurim brand of magaldrate specifications and serves as a tool for batch-level quality control.
Eurim brand of magaldrate CoA mostly includes findings from lab analyses of a specific batch. For each Eurim brand of magaldrate 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.
Eurim brand of magaldrate may be tested according to a variety of international standards, such as European Pharmacopoeia (Eurim brand of magaldrate EP), Eurim brand of magaldrate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Eurim brand of magaldrate USP).