Synopsis
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USDMF
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JDMF
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VMF
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FDA Orange Book
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Europe
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Australia
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South Africa
DRUG PRODUCT COMPOSITIONS
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1. Apo Domperidone
2. Apo-domperidone
3. Domidon
4. Domperidon
5. Domperidon Al
6. Domperidon Hexal
7. Domperidon Stada
8. Domperidon Teva
9. Domperidon-teva
10. Domperidona Gamir
11. Domperidone
12. Domperidone Maleate (1:1)
13. Domperidone Monohydrochloride
14. Gamir, Domperidona
15. Gastrocure
16. Hexal, Domperidon
17. Maleate, Domperidone
18. Monohydrochloride, Domperidone
19. Motilium
20. Nauzelin
21. Novo Domperidone
22. Novo-domperidone
23. Nu Domperidone
24. Nu-domperidone
25. Pridys
26. Pms Domperidone
27. Pms-domperidone
28. R-33,812
29. R-33812
30. R33,812
31. R33812
32. Ratio Domperidone
33. Ratio-domperidone
34. Stada, Domperidon
1. 83898-65-1
2. 99497-03-7
3. 899u5wf46a
4. 5-chloro-1-[1-[3-(2,3-dihydro-2-oxo-1h-benzimidazol-1-yl)propyl]piperidin-4-yl]-1,3-dihydro-2h-benzimidazol-2-one Maleate
5. (z)-but-2-enedioic Acid;6-chloro-3-[1-[3-(2-oxo-3h-benzimidazol-1-yl)propyl]piperidin-4-yl]-1h-benzimidazol-2-one
6. Prestwick-06g02
7. Chebi:59812
8. 2h-benzimidazol-2-one,5-chloro-1-[1-[3-(2,3-dihydro-2-oxo-1h-benzimidazol-1-yl)propyl]-4-piperidinyl]-1,3-dihydro-, (2z)-2-butenedioate
9. 5-chloro-1-(1-(3-(2,3-dihydro-2-oxo-1h-benzimidazol-1-yl)propyl)piperidin-4-yl)-1,3-dihydro-2h-benzimidazol-2-one Maleate
10. Unii-899u5wf46a
11. Domperidone (tn)
12. Einecs 281-277-7
13. Schembl447643
14. Chembl3436365
15. Domperidone (as Maleate)
16. Hy-b0411a
17. Dtxsid901019221
18. Domperidone Maleate [mart.]
19. Zda49703
20. Domperidone Maleate [who-dd]
21. Mfcd07370074
22. Akos025312518
23. Ncgc00017157-01
24. 5-chloro-1-(1-(3-(2-oxo-2,3-dihydro-1h-benzo[d]imidazol-1-yl)propyl)piperidin-4-yl)-1h-benzo[d]imidazol-2(3h)-one Maleate
25. Domperidone Maleate [ep Monograph]
26. Cs-0013583
27. D07868
28. 497d037
29. Q27126907
30. 5-chloro-1-(1-(3-(2-oxobenzimidazolin-1-yl)propyl)-4-piperidyl)benzimidazolin-2-one Maleate
| Molecular Weight | 542.0 g/mol |
|---|---|
| Molecular Formula | C26H28ClN5O6 |
| Hydrogen Bond Donor Count | 4 |
| Hydrogen Bond Acceptor Count | 7 |
| Rotatable Bond Count | 7 |
| Exact Mass | 541.1728113 g/mol |
| Monoisotopic Mass | 541.1728113 g/mol |
| Topological Polar Surface Area | 143 Ų |
| Heavy Atom Count | 38 |
| Formal Charge | 0 |
| Complexity | 774 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 1 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 2 |
Antiemetics
Drugs used to prevent NAUSEA or VOMITING. (See all compounds classified as Antiemetics.)
Dopamine Antagonists
Drugs that bind to but do not activate DOPAMINE RECEPTORS, thereby blocking the actions of dopamine or exogenous agonists. Many drugs used in the treatment of psychotic disorders (ANTIPSYCHOTIC AGENTS) are dopamine antagonists, although their therapeutic effects may be due to long-term adjustments of the brain rather than to the acute effects of blocking dopamine receptors. Dopamine antagonists have been used for several other clinical purposes including as ANTIEMETICS, in the treatment of Tourette syndrome, and for hiccup. Dopamine receptor blockade is associated with NEUROLEPTIC MALIGNANT SYNDROME. (See all compounds classified as Dopamine Antagonists.)
API SUPPLIERS
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CEP/COS
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API Imports and Exports
| Importing Country | Total Quantity (KGS) |
Average Price (USD/KGS) |
Number of Transactions |
|---|
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INTERMEDIATE SUPPLIERS
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]FDF Dossiers
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Market Place
REF. STANDARDS & IMPURITIES
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PharmaCompass offers a list of Domperidone Maleate 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 Domperidone Maleate manufacturer or Domperidone Maleate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Domperidone Maleate manufacturer or Domperidone Maleate supplier.
PharmaCompass also assists you with knowing the Domperidone Maleate API Price utilized in the formulation of products. Domperidone Maleate API Price is not always fixed or binding as the Domperidone Maleate Price is obtained through a variety of data sources. The Domperidone Maleate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Domperidone (TN) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Domperidone (TN), including repackagers and relabelers. The FDA regulates Domperidone (TN) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Domperidone (TN) 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 Domperidone (TN) manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Domperidone (TN) supplier is an individual or a company that provides Domperidone (TN) active pharmaceutical ingredient (API) or Domperidone (TN) finished formulations upon request. The Domperidone (TN) suppliers may include Domperidone (TN) API manufacturers, exporters, distributors and traders.
click here to find a list of Domperidone (TN) suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information 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 Domperidone (TN) Drug Master File in Korea (Domperidone (TN) KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Domperidone (TN). The MFDS reviews the Domperidone (TN) KDMF as part of the drug registration process and uses the information provided in the Domperidone (TN) KDMF to evaluate the safety and efficacy of the drug.
After submitting a Domperidone (TN) 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 Domperidone (TN) API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Domperidone (TN) suppliers with KDMF on PharmaCompass.
A Domperidone (TN) CEP of the European Pharmacopoeia monograph is often referred to as a Domperidone (TN) Certificate of Suitability (COS). The purpose of a Domperidone (TN) CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Domperidone (TN) EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Domperidone (TN) to their clients by showing that a Domperidone (TN) CEP has been issued for it. The manufacturer submits a Domperidone (TN) CEP (COS) as part of the market authorization procedure, and it takes on the role of a Domperidone (TN) CEP holder for the record. Additionally, the data presented in the Domperidone (TN) CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Domperidone (TN) DMF.
A Domperidone (TN) CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Domperidone (TN) CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of Domperidone (TN) suppliers with CEP (COS) on PharmaCompass.
A Domperidone (TN) written confirmation (Domperidone (TN) WC) is an official document issued by a regulatory agency to a Domperidone (TN) manufacturer, verifying that the manufacturing facility of a Domperidone (TN) active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Domperidone (TN) APIs or Domperidone (TN) finished pharmaceutical products to another nation, regulatory agencies frequently require a Domperidone (TN) WC (written confirmation) as part of the regulatory process.
click here to find a list of Domperidone (TN) suppliers with Written Confirmation (WC) on PharmaCompass.
National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Domperidone (TN) as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Domperidone (TN) API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture Domperidone (TN) as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain Domperidone (TN) and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Domperidone (TN) NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Domperidone (TN) suppliers with NDC on PharmaCompass.
Domperidone (TN) 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 Domperidone (TN) 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 Domperidone (TN) GMP manufacturer or Domperidone (TN) GMP API supplier for your needs.
A Domperidone (TN) CoA (Certificate of Analysis) is a formal document that attests to Domperidone (TN)'s compliance with Domperidone (TN) specifications and serves as a tool for batch-level quality control.
Domperidone (TN) CoA mostly includes findings from lab analyses of a specific batch. For each Domperidone (TN) 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.
Domperidone (TN) may be tested according to a variety of international standards, such as European Pharmacopoeia (Domperidone (TN) EP), Domperidone (TN) JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Domperidone (TN) USP).
