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1. 4-amino-5-chloro-2-ethoxy-n-((4-(4-fluorobenzyl)-2-morpholinyl)methyl)benzamide
2. As 4370
3. As-4370
4. Mosapride
5. Mosapride Ui05msp015ct
1. 112885-42-4
2. Gasmotin
3. As-4370
4. Mosapride (citrate)
5. Tak-370
6. Rimopride Citrate
7. 4-amino-5-chloro-2-ethoxy-n-((4-(4-fluorobenzyl)morpholin-2-yl)methyl)benzamide 2-hydroxypropane-1,2,3-tricarboxylate
8. Gasmot
9. Mf497j489p
10. Dsstox_cid_26207
11. Dsstox_rid_81436
12. Dsstox_gsid_46207
13. 4-amino-5-chloro-2-ethoxy-n-[[4-[(4-fluorophenyl)methyl]morpholin-2-yl]methyl]benzamide Citrate
14. Cas-112885-42-4
15. C21h25clfn3o3.c6h8o7
16. Unii-mf497j489p
17. Gasmotin Citrate
18. Tak-370 Citrate
19. As-4370 Citrate
20. Mosapride Citrate- Bio-x
21. (+-)-4-amino-5-chloro-2-ethoxy-n-((4-(4-fluorobenzyl)-2-morpholinyl)methyl)benzamide Citrate
22. Mls006011997
23. Schembl258620
24. Mosapride Citrate [mi]
25. Tak370
26. Chembl1733174
27. Dtxsid7046207
28. Hy-b0189a
29. Amy8852
30. Tak 370
31. Hms2051p15
32. Hms2234k07
33. Hms3369k19
34. Hms3393p15
35. Hms3651o09
36. Hms3884e13
37. Mosapride Citrate [who-dd]
38. Bcp08880
39. Tox21_111874
40. Mfcd01666680
41. Mosapride Citrate - Adooq Bioscience
42. S1385
43. Akos015895400
44. Tox21_111874_1
45. Ccg-100966
46. Ccg-270241
47. Nc00216
48. Ncgc00160527-03
49. As-13388
50. Benzamide, 4-amino-5-chloro-2-ethoxy-n-((4-((4-fluorophenyl)methyl)-2-morpholinyl)methyl)-, 2-hydroxy-1,2,3-propanetricarboxylate (1:1)
51. Bm164611
52. Sw197596-2
53. 85m424
54. D70344
55. A921736
56. Q27283985
57. (+/-)-4-amino-5-chloro-2-ethoxy-n-((4-(p-fluorobenzyl)-2-morpholinyl)methyl)benzamide Citrate
58. 4-amino-5-chloro-2-ethoxy-n-[[4-[(4 -fluorophenyl)methyl]-2-morpholinyl]methyl]benzami De Citrate
59. 4-amino-5-chloro-2-ethoxy-n-[[4-[(4-fluorophenyl)methyl]-2-morpholinyl]methyl]benzamide Citrate
60. 4-amino-5-chloro-2-ethoxy-n-[[4-[(4-fluorophenyl)methyl]morpholin-2-yl]methyl]benzamide;2-hydroxypropane-1,2,3-tricarboxylic Acid.
61. Tak-370 Citrate; As-4370 Citrat;tak370 Citrate; As4370 Citrat;tak 370 Citrate; As 4370 Citrat
| Molecular Weight | 614.0 g/mol |
|---|---|
| Molecular Formula | C27H33ClFN3O10 |
| Hydrogen Bond Donor Count | 6 |
| Hydrogen Bond Acceptor Count | 13 |
| Rotatable Bond Count | 12 |
| Exact Mass | 613.1838501 g/mol |
| Monoisotopic Mass | 613.1838501 g/mol |
| Topological Polar Surface Area | 209 Ų |
| Heavy Atom Count | 42 |
| Formal Charge | 0 |
| Complexity | 749 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 1 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 2 |
Serotonin Receptor Agonists
Endogenous compounds and drugs that bind to and activate SEROTONIN RECEPTORS. Many serotonin receptor agonists are used as ANTIDEPRESSANTS; ANXIOLYTICS; and in the treatment of MIGRAINE DISORDERS. (See all compounds classified as Serotonin Receptor Agonists.)
Gastrointestinal Agents
Drugs used for their effects on the gastrointestinal system, as to control gastric acidity, regulate gastrointestinal motility and water flow, and improve digestion. (See all compounds classified as Gastrointestinal Agents.)
API SUPPLIERS
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DKSH is your trusted partner for companies looking to grow their business in Asia & beyond.
About the Company : DKSH, founded with the goal of improving people's lives, assists businesses with market expansion and business growth in both existing and emerging markets. It has been fostering g...
Zeon Pharma is a manufacturer and supplier of APIs & Intermediates.
About the Company : Zeon Pharma Industries India Pvt ltd is an ISO & GMP certified manufacturer of Bulk drugs & Intermediate and also supplies our associate manufacturing plant API / Semi finish form...
About the Company : Fuan Pharmaceutical (Group) Co., Ltd. was established on February 25, 2004. The company is located in Chongqing Changshou Economic and Technological Development Zone, covering an a...
About the Company : Guangzhou Tosun Pharmaceutical was founded in 1999, which mainly focuses on importation & exportation of Active Pharmaceutical Ingrediants, Chemical Raw Materials, Intermediate, Ex...
About the Company : Since its foundation in 1959, JEIL Pharm established. its own central research laboratory for the formulation and synthesis of drugs, followed by its successive construction of KGM...
About the Company : Lunan Pharmaceutical Group is an integrated pharmaceutical group setting production, scientific research and sale of traditional Chinese medicines, chemicals, biological products i...
About the Company : Polaris AI Pharma is a dynamic company specializing in innovative pharmaceutical solutions. Leveraging cutting-edge AI technology, it focuses on drug discovery, development, and op...
About the Company : Sharon Bio-Medicine Limited is a fast growing Indian Pharmaceutical, Company listed at Bombay Stock Exchange. It is involved in manufacturing of Intermediates, Active Pharmaceutica...
About the Company : Symed Labs Ltd is a leading Hyderabad based manufacturer of Active Pharmaceutical Ingredients (APIs) and an end-to-end solution provider for the pharmaceutical industry for chemist...
About the Company : Viyash, true to its name, literally represents honesty and leadership in every sense. We are an integrated pharmaceutical company with a strong portfolio of niche formulations, ...
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PharmaCompass offers a list of Mosapride Citrate 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 Mosapride Citrate manufacturer or Mosapride Citrate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Mosapride Citrate manufacturer or Mosapride Citrate supplier.
PharmaCompass also assists you with knowing the Mosapride Citrate API Price utilized in the formulation of products. Mosapride Citrate API Price is not always fixed or binding as the Mosapride Citrate Price is obtained through a variety of data sources. The Mosapride Citrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Gasmot manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Gasmot, including repackagers and relabelers. The FDA regulates Gasmot manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Gasmot 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 Gasmot manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Gasmot supplier is an individual or a company that provides Gasmot active pharmaceutical ingredient (API) or Gasmot finished formulations upon request. The Gasmot suppliers may include Gasmot API manufacturers, exporters, distributors and traders.
click here to find a list of Gasmot suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Gasmot DMF (Drug Master File) is a document detailing the whole manufacturing process of Gasmot active pharmaceutical ingredient (API) in detail. Different forms of Gasmot DMFs exist exist since differing nations have different regulations, such as Gasmot USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Gasmot DMF submitted to regulatory agencies in the US is known as a USDMF. Gasmot USDMF includes data on Gasmot's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Gasmot USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Gasmot suppliers with USDMF on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Gasmot Drug Master File in Japan (Gasmot JDMF) empowers Gasmot API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Gasmot JDMF during the approval evaluation for pharmaceutical products. At the time of Gasmot JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Gasmot suppliers with JDMF on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Gasmot Drug Master File in Korea (Gasmot KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Gasmot. The MFDS reviews the Gasmot KDMF as part of the drug registration process and uses the information provided in the Gasmot KDMF to evaluate the safety and efficacy of the drug.
After submitting a Gasmot KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their Gasmot API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Gasmot suppliers with KDMF on PharmaCompass.
A Gasmot written confirmation (Gasmot WC) is an official document issued by a regulatory agency to a Gasmot manufacturer, verifying that the manufacturing facility of a Gasmot active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Gasmot APIs or Gasmot finished pharmaceutical products to another nation, regulatory agencies frequently require a Gasmot WC (written confirmation) as part of the regulatory process.
click here to find a list of Gasmot suppliers with Written Confirmation (WC) on PharmaCompass.
Gasmot 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 Gasmot 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 Gasmot GMP manufacturer or Gasmot GMP API supplier for your needs.
A Gasmot CoA (Certificate of Analysis) is a formal document that attests to Gasmot's compliance with Gasmot specifications and serves as a tool for batch-level quality control.
Gasmot CoA mostly includes findings from lab analyses of a specific batch. For each Gasmot 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.
Gasmot may be tested according to a variety of international standards, such as European Pharmacopoeia (Gasmot EP), Gasmot JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Gasmot USP).
