Synopsis
Synopsis
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JDMF
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NDC API
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EDQM
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USP
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JP
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FDA Orange Book
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Europe
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Canada
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Australia
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1. 5-diethylaminoethyl-3-phenyl-1,2,4-oxadiazole
2. Bredon
3. Oxobron
4. Oxolamine Citrate
5. Oxolamine Monohydrochloride
1. 959-14-8
2. N,n-diethyl-2-(3-phenyl-1,2,4-oxadiazol-5-yl)ethanamine
3. Oxolamina
4. Oksalamin
5. 683 M
6. Af 438
7. Oxadiazole; 683m
8. 5-(2-diethylaminoethyl)-3-phenyl-1,2,4-oxadiazole
9. Af-438 Free Base
10. N,n-diethyl-3-phenyl-1,2,4-oxadiazole-5-ethanamine
11. 90bea145gy
12. Skf 9976 Free Base
13. Skf-9976 Free Base
14. Af-438 [as Citrate]
15. Oxolamine (inn)
16. Skf 9976 [as Citrate]
17. 5-(2-dietilaminoetil)-3-fenil-1,2,4-oxadiazolo
18. Oxolamine [inn]
19. Oxolev
20. Jatan
21. 1,2,4-oxadiazole, 5-(2-(diethylamino)ethyl)-3-phenyl-
22. Oxolev A
23. Ossolamina [dcit]
24. Oxolamina [italian]
25. Ossolamina
26. Oxolaminum
27. Oxolamine [inn:dcf]
28. N,n-diethyl-2-(3-phenyl-1,2,4-oxadiazol-5-yl)ethan-1-amine
29. Oxolaminum [inn-latin]
30. Oxolamina [inn-spanish]
31. Einecs 213-493-4
32. Brn 0527181
33. Unii-90bea145gy
34. Oksalamin (tn)
35. 3-phenyl-5-(beta-diethylaminoethyl)-1,2,4-oxodiazole
36. 5-(2-dietilaminoetil)-3-fenil-1,2,4-oxadiazolo [italian]
37. Oxolamine [mi]
38. Prestwick0_000826
39. Prestwick1_000826
40. Prestwick2_000826
41. Prestwick3_000826
42. Oxolamine [mart.]
43. Ec 213-493-4
44. Oxolamine [who-dd]
45. Bspbio_000751
46. Schembl893333
47. Spbio_002672
48. Bpbio1_000827
49. Zinc1874
50. 1,2,4-oxadiazole-5-ethanamine, N,n-diethyl-3-phenyl-
51. Chembl1620875
52. Dtxsid5023403
53. Chebi:94607
54. Db13216
55. Ncgc00179449-01
56. Sbi-0207016.p001
57. Ft-0748644
58. D07387
59. 959o148
60. Q576684
61. Brd-k42596464-048-03-6
62. 3-phenyl-5-(.beta.-diethylaminoethyl)-1,2,4-oxodiazole
63. N,n-diethyl-2-(3-phenyl-1,2,4-oxadiazol-5-yl)ethanamine 2-hydroxy-1,2,3-propanetricarboxylate
| Molecular Weight | 245.32 g/mol |
|---|---|
| Molecular Formula | C14H19N3O |
| XLogP3 | 2.9 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 6 |
| Exact Mass | 245.152812238 g/mol |
| Monoisotopic Mass | 245.152812238 g/mol |
| Topological Polar Surface Area | 42.2 Ų |
| Heavy Atom Count | 18 |
| Formal Charge | 0 |
| Complexity | 227 |
| 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 |
Antitussive Agents
Agents that suppress cough. They act centrally on the medullary cough center. EXPECTORANTS, also used in the treatment of cough, act locally. (See all compounds classified as Antitussive Agents.)
R - Respiratory system
R05 - Cough and cold preparations
R05D - Cough suppressants, excl. combinations with expectorants
R05DB - Other cough suppressants
R05DB07 - Oxolamine
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| Importing Country | Total Quantity (KGS) |
Average Price (USD/KGS) |
Number of Transactions |
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PharmaCompass offers a list of Oxolamine 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 Oxolamine manufacturer or Oxolamine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Oxolamine manufacturer or Oxolamine supplier.
PharmaCompass also assists you with knowing the Oxolamine API Price utilized in the formulation of products. Oxolamine API Price is not always fixed or binding as the Oxolamine Price is obtained through a variety of data sources. The Oxolamine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Oxolamine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Oxolamine, including repackagers and relabelers. The FDA regulates Oxolamine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Oxolamine 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 Oxolamine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Oxolamine supplier is an individual or a company that provides Oxolamine active pharmaceutical ingredient (API) or Oxolamine finished formulations upon request. The Oxolamine suppliers may include Oxolamine API manufacturers, exporters, distributors and traders.
click here to find a list of Oxolamine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Oxolamine written confirmation (Oxolamine WC) is an official document issued by a regulatory agency to a Oxolamine manufacturer, verifying that the manufacturing facility of a Oxolamine active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Oxolamine APIs or Oxolamine finished pharmaceutical products to another nation, regulatory agencies frequently require a Oxolamine WC (written confirmation) as part of the regulatory process.
click here to find a list of Oxolamine suppliers with Written Confirmation (WC) on PharmaCompass.
Oxolamine 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 Oxolamine 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 Oxolamine GMP manufacturer or Oxolamine GMP API supplier for your needs.
A Oxolamine CoA (Certificate of Analysis) is a formal document that attests to Oxolamine's compliance with Oxolamine specifications and serves as a tool for batch-level quality control.
Oxolamine CoA mostly includes findings from lab analyses of a specific batch. For each Oxolamine 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.
Oxolamine may be tested according to a variety of international standards, such as European Pharmacopoeia (Oxolamine EP), Oxolamine JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Oxolamine USP).
