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1. Methopromazine Maleate (1:1)
2. Methopromazine Maleate (1:2)
3. Methoxypromazine
1. Methoxypromazine
2. Neoproma
3. Tenton
4. Tentone
5. 61-01-8
6. 2-methoxypromazine
7. 2-methoxy Promazine
8. Methopromazine [inn]
9. Rp 4632
10. 2-methoxy-10-(3'-dimethylaminopropyl)phenothiazine
11. 10-(3-dimethylaminopropyl)-2-methoxyphenothiazine
12. A6f645q9hq
13. 3-(2-methoxyphenothiazin-10-yl)-n,n-dimethylpropan-1-amine
14. 10h-phenothiazine-10-propanamine, 2-methoxy-n,n-dimethyl-
15. Methopromazinum
16. Metopromazina
17. Methopromazinum [inn-latin]
18. Metopromazina [inn-spanish]
19. Einecs 200-497-6
20. Unii-a6f645q9hq
21. Mopazin (salt/mix)
22. Mopazine (salt/mix)
23. Oprea1_778116
24. Methoxypromazine [mi]
25. Zinc488
26. Schembl149884
27. 10-[3-(dimethylamino)propyl]-2-methoxyphenothiazine
28. Methopromazine [who-dd]
29. Chembl2110655
30. Phenothiazine, 10-(3-(dimethylamino)propyl)-2-methoxy
31. 2-methoxy-n,n-dimethyl-10h-phenothiazine-10-propanamine
32. Dtxsid90209843
33. Chebi:135347
34. Bdbm50497149
35. 4632 R.p
36. Ft-0671071
37. Methoxypromazine Tentone,methopromazine
38. 2-methoxy-10-[3'-(dimethylamino)propyl]phenothiazine
39. Q27273690
40. Phenothiazine, 10-[3-(dimethylamino)propyl]-2-methoxy-
41. 3-(2-methoxy-10h-phenothiazin-10-yl)-n,n-dimethyl-1-propanamine #
| Molecular Weight | 314.4 g/mol |
|---|---|
| Molecular Formula | C18H22N2OS |
| XLogP3 | 4.9 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 5 |
| Exact Mass | 314.14528450 g/mol |
| Monoisotopic Mass | 314.14528450 g/mol |
| Topological Polar Surface Area | 41 Ų |
| Heavy Atom Count | 22 |
| Formal Charge | 0 |
| Complexity | 352 |
| 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 | 1 |
INTERMEDIATES SUPPLIERS
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]ABOUT THIS PAGE
A Methopromazine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Methopromazine, including repackagers and relabelers. The FDA regulates Methopromazine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Methopromazine 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 Methopromazine supplier is an individual or a company that provides Methopromazine active pharmaceutical ingredient (API) or Methopromazine finished formulations upon request. The Methopromazine suppliers may include Methopromazine API manufacturers, exporters, distributors and traders.
Methopromazine 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 Methopromazine 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 Methopromazine GMP manufacturer or Methopromazine GMP API supplier for your needs.
A Methopromazine CoA (Certificate of Analysis) is a formal document that attests to Methopromazine's compliance with Methopromazine specifications and serves as a tool for batch-level quality control.
Methopromazine CoA mostly includes findings from lab analyses of a specific batch. For each Methopromazine 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.
Methopromazine may be tested according to a variety of international standards, such as European Pharmacopoeia (Methopromazine EP), Methopromazine JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Methopromazine USP).
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