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1. Meglumine Antimoniate
2. N Methylglucamine Antimonate
3. N-methylglucamine Antimonate
1. Meglumine Antimonate
2. Meglumine Antimoniate
3. N-methylglucamine Antimonate
4. 133-51-7
5. Methylglucamine Antimonate
6. Protostib
7. 75g4tw236w
8. N-methyl Glucamine Antimoniate
9. 2168-rp
10. Einecs 205-108-3
11. Glucantim
12. Unii-75g4tw236w
13. 1-deoxy-1-(methylamino)glucitol Antimonate(v)
14. 1-deoxy-1-(methylamino)-d-glucitol, Compound With Antimonic Acid (1:1)
15. D-glucitol, 1-deoxy-1-(methylamino)-, Compd. With Antimonic Acid (1:1)
16. Glucitol, 1-deoxy-1-(methylamino)-, Compd. With Antimonic Acid (1:1), D-
17. Schembl146372
18. Dtxsid4043935
19. D-glucitol, 1-deoxy-1-(methylamino)-, Trioxoantimonate(1-)
20. Mfcd01725422
21. Meglumine Antimonate [who-dd]
22. Akos025310684
23. Db13732
24. N-methylglucamine Antimonate [mi]
25. 133m517
26. Q2757969
27. (2r,3r,4r,5s)-6-(methylamino)hexane-1,2,3,4,5-pentaol Stibenate
28. D-glucitol, 1-deoxy-1-(methylamino)-, Compd. With Antimonic Acid (hsbo3) (1:1)
Molecular Weight | 365.98 g/mol |
---|---|
Molecular Formula | C7H18NO8Sb |
Hydrogen Bond Donor Count | 7 |
Hydrogen Bond Acceptor Count | 9 |
Rotatable Bond Count | 6 |
Exact Mass | 365.00705 g/mol |
Monoisotopic Mass | 365.00705 g/mol |
Topological Polar Surface Area | 168 Ų |
Heavy Atom Count | 17 |
Formal Charge | 0 |
Complexity | 180 |
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 | 2 |
Antiprotozoal Agents
Substances that are destructive to protozoans. (See all compounds classified as Antiprotozoal Agents.)
P - Antiparasitic products, insecticides and repellents
P01 - Antiprotozoals
P01C - Agents against leishmaniasis and trypanosomiasis
P01CB - Antimony compounds
P01CB01 - Meglumine antimonate
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ABOUT THIS PAGE
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PharmaCompass offers a list of Meglumine Antimonate 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 Meglumine Antimonate manufacturer or Meglumine Antimonate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Meglumine Antimonate manufacturer or Meglumine Antimonate supplier.
PharmaCompass also assists you with knowing the Meglumine Antimonate API Price utilized in the formulation of products. Meglumine Antimonate API Price is not always fixed or binding as the Meglumine Antimonate Price is obtained through a variety of data sources. The Meglumine Antimonate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A N Methylglucamine Antimonate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of N Methylglucamine Antimonate, including repackagers and relabelers. The FDA regulates N Methylglucamine Antimonate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. N Methylglucamine Antimonate 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 N Methylglucamine Antimonate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A N Methylglucamine Antimonate supplier is an individual or a company that provides N Methylglucamine Antimonate active pharmaceutical ingredient (API) or N Methylglucamine Antimonate finished formulations upon request. The N Methylglucamine Antimonate suppliers may include N Methylglucamine Antimonate API manufacturers, exporters, distributors and traders.
click here to find a list of N Methylglucamine Antimonate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A N Methylglucamine Antimonate DMF (Drug Master File) is a document detailing the whole manufacturing process of N Methylglucamine Antimonate active pharmaceutical ingredient (API) in detail. Different forms of N Methylglucamine Antimonate DMFs exist exist since differing nations have different regulations, such as N Methylglucamine Antimonate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A N Methylglucamine Antimonate DMF submitted to regulatory agencies in the US is known as a USDMF. N Methylglucamine Antimonate USDMF includes data on N Methylglucamine Antimonate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The N Methylglucamine Antimonate USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of N Methylglucamine Antimonate suppliers with USDMF on PharmaCompass.
N Methylglucamine Antimonate 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 N Methylglucamine Antimonate 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 N Methylglucamine Antimonate GMP manufacturer or N Methylglucamine Antimonate GMP API supplier for your needs.
A N Methylglucamine Antimonate CoA (Certificate of Analysis) is a formal document that attests to N Methylglucamine Antimonate's compliance with N Methylglucamine Antimonate specifications and serves as a tool for batch-level quality control.
N Methylglucamine Antimonate CoA mostly includes findings from lab analyses of a specific batch. For each N Methylglucamine Antimonate 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.
N Methylglucamine Antimonate may be tested according to a variety of international standards, such as European Pharmacopoeia (N Methylglucamine Antimonate EP), N Methylglucamine Antimonate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (N Methylglucamine Antimonate USP).