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1. Cervilane
1. 10226-54-7
2. 1,3-dimethyl-7-(5-oxohexyl)-1h-purine-2,6(3h,7h)-dione
3. Lomifylline [inn]
4. 7-(5-oxohexyl)theophylline
5. 1,3-dimethyl-7-(5-oxohexyl)purine-2,6-dione
6. Na91gv8gdj
7. Lomifilina
8. Lomifyllinum
9. Smr000466379
10. Unii-na91gv8gdj
11. Lomifilina [inn-spanish]
12. Lomifyllinum [inn-latin]
13. Einecs 233-547-0
14. Lomifylline [mart.]
15. Lomifylline [who-dd]
16. Mls000759512
17. Mls001424104
18. Chembl311948
19. Schembl1649451
20. Chebi:94702
21. Dtxsid10144848
22. Hms2051p03
23. Hms3393p03
24. 1,2,3,6-tetrahydro-1,3-dimethyl-7-(5-oxohexyl)purin-2,6-dion
25. Zinc2020029
26. 7-(5-oxohexyl)-1,3-dimethylxanthine
27. Akos016013999
28. Ccg-100918
29. Nc00168
30. Sb67404
31. 1,3-dimethyl-7-(5-oxohexyl)-xanthine
32. 7-(5-keto-hexyl)-1,3-dimethylxanthine
33. Ncgc00246970-01
34. Ft-0630377
35. L-a-amino-g-guanidinobutyricacidhydrochloride
36. Q27166504
37. 1,3-dimethyl-7-(5-oxo-hexyl)-3,7-dihydro-purine-2,6-dione
38. 1,3-dimethyl-7-(5-oxohexyl)-3,7-dihydro-1h-purine-2,6-dione
39. 3,7-dihydro-1,3-dimethyl-7-(5-oxohexyl)-1h-purine-2,6-dione
40. Purin-2,6-dione, 1,2,3,6-tetrahydro-1,3-dimethyl-7-(5-oxohexyl)-
| Molecular Weight | 278.31 g/mol |
|---|---|
| Molecular Formula | C13H18N4O3 |
| XLogP3 | -0.1 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 5 |
| Exact Mass | 278.13789045 g/mol |
| Monoisotopic Mass | 278.13789045 g/mol |
| Topological Polar Surface Area | 75.5 Ų |
| Heavy Atom Count | 20 |
| Formal Charge | 0 |
| Complexity | 426 |
| 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 |
ABOUT THIS PAGE
A Lomifylline manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lomifylline, including repackagers and relabelers. The FDA regulates Lomifylline manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lomifylline 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 Lomifylline manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Lomifylline supplier is an individual or a company that provides Lomifylline active pharmaceutical ingredient (API) or Lomifylline finished formulations upon request. The Lomifylline suppliers may include Lomifylline API manufacturers, exporters, distributors and traders.
click here to find a list of Lomifylline suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
Lomifylline 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 Lomifylline 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 Lomifylline GMP manufacturer or Lomifylline GMP API supplier for your needs.
A Lomifylline CoA (Certificate of Analysis) is a formal document that attests to Lomifylline's compliance with Lomifylline specifications and serves as a tool for batch-level quality control.
Lomifylline CoA mostly includes findings from lab analyses of a specific batch. For each Lomifylline 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.
Lomifylline may be tested according to a variety of international standards, such as European Pharmacopoeia (Lomifylline EP), Lomifylline JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Lomifylline USP).
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