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1. 4-(ethyl-(4-methoxy-alpha-methylphenethyl)aminobutyl) Veratrate
2. Duspatalin
3. Mebeverine
4. Spasmotalin
1. 2753-45-9
2. Mebeverine Hcl
3. Duspatalin
4. Colofac
5. Csag-144
6. Csag 144
7. Mebeverine Hydrochloride [usan]
8. Mebeverine (hydrochloride)
9. Nsc-169101
10. 15vz5al4jn
11. 4-[ethyl-[1-(4-methoxyphenyl)propan-2-yl]amino]butyl 3,4-dimethoxybenzoate;hydrochloride
12. Mls000028652
13. Duspatal
14. Benzoic Acid, 3,4-dimethoxy-, 4-(ethyl(2-(4-methoxyphenyl)-1-methylethyl)amino)butyl Ester, Hydrochloride
15. Rudakol
16. Smr000058862
17. Dsstox_cid_25372
18. Dsstox_rid_80834
19. Dsstox_gsid_45372
20. Mebeverine Hydrochloride (usan)
21. 4-(ethyl(1-(4-methoxyphenyl)propan-2-yl)amino)butyl 3,4-dimethoxybenzoate Hydrochloride
22. 4-{ethyl[2-(4-methoxyphenyl)-1-methylethyl]amino}butyl 3,4-dimethoxybenzoate Hydrochloride
23. Nsc 169101
24. Nsc169101
25. Einecs 220-400-0
26. Unii-15vz5al4jn
27. Sr-01000003159
28. 4-(ethyl(p-methoxy-.alpha.-methylphenethyl)amino)butyl Veratrate Hydrochloride
29. 4-[ethyl(p-methoxy-.alpha.-methylphenethyl)amino]butyl Veratrate Hydrochloride
30. Prestwick_587
31. Mebeverine D6 Hcl
32. Colofac Hydrochloride
33. Duspatal Hydrochloride
34. Duspatalin Hydrochloride
35. Opera_id_1589
36. Ncgc00016617-01
37. 4-(ethyl(p-methoxy-alpha-methylphenethyl)amino)butyl Veratrate Hydrochloride
38. Cas-2753-45-9
39. Mls001148590
40. Mls002222299
41. Schembl121977
42. Spectrum1501117
43. Regid_for_cid_17683
44. Chembl1446650
45. Dtxsid1045372
46. Hms1568n22
47. Hms1921f15
48. Pharmakon1600-01501117
49. Bcp28149
50. Ex-a4568
51. Hy-a0078
52. Tox21_110527
53. Ccg-39022
54. Mebeverine Hydrochloride [mi]
55. Mfcd00083411
56. Nsc757840
57. S5027
58. Akos027420570
59. Tox21_110527_1
60. Cs-6931
61. Nsc-757840
62. 4-[ethyl-[1-(4-methoxyphenyl)propan-2-yl]amino]butyl 3,4-dimethoxybenzoate Hydrochloride
63. Mebeverine Hydrochloride [mart.]
64. Veratric Acid, 4-(ethyl(p-methoxy-alpha-methylphenethyl)amino)butyl Ester, Hydrochloride
65. Mebeverine Hydrochloride [who-dd]
66. Ncgc00018277-06
67. Ncgc00094900-01
68. Ncgc00094900-02
69. Ncgc00094900-03
70. 3,4-dimethoxybenzoic Acid 4-[ethyl[2-(4-methoxyphenyl)-1-methylethyl]amino]butyl Ester Hydrochloride
71. Veratric Acid, Butyl Ester, Hydrochloride
72. Db-047240
73. Ft-0603620
74. Mebeverine Hydrochloride, Analytical Standard
75. D04868
76. Mebeverine Hydrochloride [ep Monograph]
77. N16922
78. Wln: 1or Bo1 Dvo4n2&y1&1r Do1 &gh
79. 753m459
80. A819105
81. Sr-01000003159-4
82. W-109821
83. Mebeverine Hcl Pound>>csag-144 Pound>>csag 144 Pound>>csag144
84. 3,4-dimethoxybenzoicacid4-ethyl2-(4-methoxyphenyl)-1-methylethylaminobutylesterhydrochloride
85. 4-(ethyl(1-(4-methoxyphenyl)propan-2-yl)amino)butyl3,4-dimethoxybenzoatehydrochloride
86. Veratric Acid, 4-[ethyl(p-methoxy-.alpha.-methylphenethyl)amino]butyl Ester Hydrochloride
87. 3,4-dimethoxybenzoic Acid 4-[ethyl-[1-(4-methoxyphenyl)propan-2-yl]amino]butyl Ester Hydrochloride
88. Benzoic Acid,4-dimethoxy-, 4-[ethyl[2-(4-methoxyphenyl)-1-methylethyl]amino]butyl Ester, Hydrochloride
| Molecular Weight | 466.0 g/mol |
|---|---|
| Molecular Formula | C25H36ClNO5 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 6 |
| Rotatable Bond Count | 14 |
| Exact Mass | 465.2282009 g/mol |
| Monoisotopic Mass | 465.2282009 g/mol |
| Topological Polar Surface Area | 57.2 Ų |
| Heavy Atom Count | 32 |
| Formal Charge | 0 |
| Complexity | 494 |
| 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 |
Parasympatholytics
Agents that inhibit the actions of the parasympathetic nervous system. The major group of drugs used therapeutically for this purpose is the MUSCARINIC ANTAGONISTS. (See all compounds classified as Parasympatholytics.)
Anticonvulsants
Drugs used to prevent SEIZURES or reduce their severity. (See all compounds classified as Anticonvulsants.)
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PharmaCompass offers a list of Mebeverine 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 Mebeverine manufacturer or Mebeverine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Mebeverine manufacturer or Mebeverine supplier.
PharmaCompass also assists you with knowing the Mebeverine API Price utilized in the formulation of products. Mebeverine API Price is not always fixed or binding as the Mebeverine Price is obtained through a variety of data sources. The Mebeverine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Rudakol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Rudakol, including repackagers and relabelers. The FDA regulates Rudakol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Rudakol 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 Rudakol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Rudakol supplier is an individual or a company that provides Rudakol active pharmaceutical ingredient (API) or Rudakol finished formulations upon request. The Rudakol suppliers may include Rudakol API manufacturers, exporters, distributors and traders.
click here to find a list of Rudakol suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Rudakol DMF (Drug Master File) is a document detailing the whole manufacturing process of Rudakol active pharmaceutical ingredient (API) in detail. Different forms of Rudakol DMFs exist exist since differing nations have different regulations, such as Rudakol USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Rudakol DMF submitted to regulatory agencies in the US is known as a USDMF. Rudakol USDMF includes data on Rudakol's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Rudakol USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Rudakol suppliers with USDMF on PharmaCompass.
A Rudakol CEP of the European Pharmacopoeia monograph is often referred to as a Rudakol Certificate of Suitability (COS). The purpose of a Rudakol CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Rudakol EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Rudakol to their clients by showing that a Rudakol CEP has been issued for it. The manufacturer submits a Rudakol CEP (COS) as part of the market authorization procedure, and it takes on the role of a Rudakol CEP holder for the record. Additionally, the data presented in the Rudakol CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Rudakol DMF.
A Rudakol CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Rudakol 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 Rudakol suppliers with CEP (COS) on PharmaCompass.
A Rudakol written confirmation (Rudakol WC) is an official document issued by a regulatory agency to a Rudakol manufacturer, verifying that the manufacturing facility of a Rudakol active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Rudakol APIs or Rudakol finished pharmaceutical products to another nation, regulatory agencies frequently require a Rudakol WC (written confirmation) as part of the regulatory process.
click here to find a list of Rudakol suppliers with Written Confirmation (WC) on PharmaCompass.
Rudakol 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 Rudakol 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 Rudakol GMP manufacturer or Rudakol GMP API supplier for your needs.
A Rudakol CoA (Certificate of Analysis) is a formal document that attests to Rudakol's compliance with Rudakol specifications and serves as a tool for batch-level quality control.
Rudakol CoA mostly includes findings from lab analyses of a specific batch. For each Rudakol 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.
Rudakol may be tested according to a variety of international standards, such as European Pharmacopoeia (Rudakol EP), Rudakol JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Rudakol USP).
