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1. Tasto
2. Trometamolgluconate Aluminum
1. Tasto
2. 13755-41-4
3. I670ei8m2n
4. Tris(hydroxymethyl)aminomethanegluconate Dihydroxyaluminate
5. Aluminum;2-amino-2-(hydroxymethyl)propane-1,3-diol;(2r,3s,4r,5r)-2,3,4,5,6-pentahydroxyhexanoate;dihydroxide
6. Unii-i670ei8m2n
7. Aloglutamol [who-dd]
8. Dtxsid601027584
9. Q4734171
10. Dihydroxyaluminum Gluconate, Tris(hydroxymethyl)aminomethane (1:1)
Molecular Weight | 377.28 g/mol |
---|---|
Molecular Formula | C10H24AlNO12 |
Hydrogen Bond Donor Count | 11 |
Hydrogen Bond Acceptor Count | 13 |
Rotatable Bond Count | 7 |
Exact Mass | 377.1113886 g/mol |
Monoisotopic Mass | 377.1113886 g/mol |
Topological Polar Surface Area | 230 Ų |
Heavy Atom Count | 24 |
Formal Charge | 0 |
Complexity | 219 |
Isotope Atom Count | 0 |
Defined Atom Stereocenter Count | 4 |
Undefined Atom Stereocenter Count | 0 |
Defined Bond Stereocenter Count | 0 |
Undefined Bond Stereocenter Count | 0 |
Covalently Bonded Unit Count | 5 |
A - Alimentary tract and metabolism
A02 - Drugs for acid related disorders
A02A - Antacids
A02AB - Aluminium compounds
A02AB06 - Aloglutamol
ABOUT THIS PAGE
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PharmaCompass offers a list of UNII-I670EI8M2N 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 UNII-I670EI8M2N manufacturer or UNII-I670EI8M2N supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred UNII-I670EI8M2N manufacturer or UNII-I670EI8M2N supplier.
PharmaCompass also assists you with knowing the UNII-I670EI8M2N API Price utilized in the formulation of products. UNII-I670EI8M2N API Price is not always fixed or binding as the UNII-I670EI8M2N Price is obtained through a variety of data sources. The UNII-I670EI8M2N Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A aloglutamol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of aloglutamol, including repackagers and relabelers. The FDA regulates aloglutamol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. aloglutamol API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A aloglutamol supplier is an individual or a company that provides aloglutamol active pharmaceutical ingredient (API) or aloglutamol finished formulations upon request. The aloglutamol suppliers may include aloglutamol API manufacturers, exporters, distributors and traders.
click here to find a list of aloglutamol suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A aloglutamol DMF (Drug Master File) is a document detailing the whole manufacturing process of aloglutamol active pharmaceutical ingredient (API) in detail. Different forms of aloglutamol DMFs exist exist since differing nations have different regulations, such as aloglutamol USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A aloglutamol DMF submitted to regulatory agencies in the US is known as a USDMF. aloglutamol USDMF includes data on aloglutamol's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The aloglutamol USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of aloglutamol suppliers with USDMF on PharmaCompass.
aloglutamol 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 aloglutamol 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 aloglutamol GMP manufacturer or aloglutamol GMP API supplier for your needs.
A aloglutamol CoA (Certificate of Analysis) is a formal document that attests to aloglutamol's compliance with aloglutamol specifications and serves as a tool for batch-level quality control.
aloglutamol CoA mostly includes findings from lab analyses of a specific batch. For each aloglutamol 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.
aloglutamol may be tested according to a variety of international standards, such as European Pharmacopoeia (aloglutamol EP), aloglutamol JP (Japanese Pharmacopeia) and the US Pharmacopoeia (aloglutamol USP).