Synopsis
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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
API SUPPLIERS
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 3248
Submission : 1978-04-11
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
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USDMF
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 3248
Submission : 1978-04-11
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]ABOUT THIS PAGE
A UNII-I670EI8M2N manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of UNII-I670EI8M2N, including repackagers and relabelers. The FDA regulates UNII-I670EI8M2N manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. UNII-I670EI8M2N 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 UNII-I670EI8M2N supplier is an individual or a company that provides UNII-I670EI8M2N active pharmaceutical ingredient (API) or UNII-I670EI8M2N finished formulations upon request. The UNII-I670EI8M2N suppliers may include UNII-I670EI8M2N API manufacturers, exporters, distributors and traders.
click here to find a list of UNII-I670EI8M2N suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A UNII-I670EI8M2N DMF (Drug Master File) is a document detailing the whole manufacturing process of UNII-I670EI8M2N active pharmaceutical ingredient (API) in detail. Different forms of UNII-I670EI8M2N DMFs exist exist since differing nations have different regulations, such as UNII-I670EI8M2N USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A UNII-I670EI8M2N DMF submitted to regulatory agencies in the US is known as a USDMF. UNII-I670EI8M2N USDMF includes data on UNII-I670EI8M2N's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The UNII-I670EI8M2N USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of UNII-I670EI8M2N suppliers with USDMF on PharmaCompass.
UNII-I670EI8M2N 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 UNII-I670EI8M2N 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 UNII-I670EI8M2N GMP manufacturer or UNII-I670EI8M2N GMP API supplier for your needs.
A UNII-I670EI8M2N CoA (Certificate of Analysis) is a formal document that attests to UNII-I670EI8M2N's compliance with UNII-I670EI8M2N specifications and serves as a tool for batch-level quality control.
UNII-I670EI8M2N CoA mostly includes findings from lab analyses of a specific batch. For each UNII-I670EI8M2N 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.
UNII-I670EI8M2N may be tested according to a variety of international standards, such as European Pharmacopoeia (UNII-I670EI8M2N EP), UNII-I670EI8M2N JP (Japanese Pharmacopeia) and the US Pharmacopoeia (UNII-I670EI8M2N USP).
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