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1. Eurax
1. 483-63-6
2. N-ethyl-o-crotonotoluidide
3. Trans-crotamiton
4. Crotamitone
5. Eurax
6. Crotalgin
7. 124236-29-9
8. Veteusan
9. Crotamitex
10. Eurasil
11. Euraxil
12. Crotamitonum
13. Crotonyl-n-ethyl-o-toluidine
14. Crotamiton, (e)-
15. 2-butenamide, N-ethyl-n-(2-methylphenyl)-
16. (e)-n-ethyl-n-(2-methylphenyl)but-2-enamide
17. (e)-n-ethyl-n-(o-tolyl)but-2-enamide
18. O-crotonotoluidide, N-ethyl-
19. (2e)-n-ethyl-n-(2-methylphenyl)but-2-enamide
20. 2eeh27851y
21. 2-butenamide, N-ethyl-n-(2-methylphenyl)-, (e)-
22. Mfcd00026989
23. 2-butenamide, N-ethyl-n-(2-methylphenyl)-, (2e)-
24. Nsc-758951
25. Crotan
26. Caswell No. 431b
27. Bestloid
28. Crotamitonum [inn-latin]
29. Smr000059145
30. N-ethyl-n-(2-methylphenyl)but-2-enamide
31. Sr-01000759366
32. Einecs 207-596-3
33. Unii-d6s4o4xd0h
34. Epa Pesticide Chemical Code 055701
35. Chebi:31439
36. Brn 3275497
37. N-ethyl-n-(2-methylphenyl)-2-butenamide
38. Unii-2eeh27851y
39. Ai3-17732
40. N-crotonyl-n-ethyl-o-toluidine
41. (e)-crotamiton
42. Crotamiton [usp:inn:ban:jan]
43. Eurax (tn)
44. Prestwick2_000951
45. Prestwick3_000951
46. N-ethylcrotono-o-toluidide
47. N-ethyl-o-crotonotoluidine
48. G 7857
49. N-ethyl- O-crotonotoluidide
50. D6s4o4xd0h
51. Schembl32934
52. Bspbio_000942
53. Bspbio_002722
54. Crotamiton (jan/usp/inn)
55. 3-12-00-01856 (beilstein Handbook Reference)
56. Mls000759489
57. Mls001424003
58. Mls002222307
59. Mls002695895
60. N-ethyl-ortho-crotonotoluidide
61. Spectrum1505271
62. Bpbio1_001038
63. Component Of Eurax (salt/mix)
64. Chembl1200709
65. Gtpl11165
66. Zinc56427
67. N-ethyl-o-crotonotoluidide, 97%
68. Dtxsid101256463
69. Hms1570p04
70. Hms1922p21
71. Hms2051e10
72. Hms2090a10
73. Hms2093o12
74. Hms2097p04
75. Hms2234e16
76. Hms3714p04
77. Pharmakon1600-01505271
78. Bcp13315
79. Hy-b1177
80. N-ethyl-n-(o-tolyl)but-2-enamide
81. Nsc78382
82. Ccg-39402
83. Nsc-78382
84. Nsc758951
85. S1711
86. (e)-n-ethyl-n-o-tolylbut-2-enamide
87. Akos015892746
88. Cs-4730
89. Nc00107
90. Nsc 758951
91. Ncgc00094571-01
92. Ncgc00094571-02
93. Ncgc00094571-03
94. Ncgc00094571-04
95. Ncgc00094571-05
96. As-11641
97. Trans-n-ethyl-n-(o-tolyl)-2-butenamide
98. Sbi-0206763.p001
99. Ab00513973
100. E0814
101. N-ethyl-n-(2-methylphenyl)-2-butenamide #
102. D01381
103. D70888
104. (2e)-n-ethyl-n-(2-methylphenyl)-2-butenamide
105. Ab00513973-09
106. Ab00513973_10
107. 483c636
108. A827519
109. Q-200893
110. Q2439845
111. Sr-01000759366-4
112. Sr-01000759366-6
113. Brd-k13240564-001-01-8
114. Brd-k57179821-001-05-5
115. Brd-k57179821-001-08-9
116. Crotamiton, British Pharmacopoeia (bp) Reference Standard
117. Crotamiton, European Pharmacopoeia (ep) Reference Standard
118. Crotamiton, United States Pharmacopeia (usp) Reference Standard
119. N-ethyl-o-crotonotoluidide; Crotamitone; Crotalgin; Eurasil; Euraxil
| Molecular Weight | 203.28 g/mol |
|---|---|
| Molecular Formula | C13H17NO |
| XLogP3 | 2.8 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 3 |
| Exact Mass | 203.131014166 g/mol |
| Monoisotopic Mass | 203.131014166 g/mol |
| Topological Polar Surface Area | 20.3 Ų |
| Heavy Atom Count | 15 |
| Formal Charge | 0 |
| Complexity | 235 |
| 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 | 1 |
| 1 of 4 | |
|---|---|
| Drug Name | Crotan |
| PubMed Health | Crotamiton (On the skin) |
| Drug Classes | Scabicide |
| Drug Label | Eurax (crotamiton USP) is a scabicidal and antipruritic agent available as a cream or lotion for topical use only. Eurax provides 10% (w/w) of the synthetic, crotamiton USP, in a vanishing-cream or emollient-lotion base containing: carbomer-934, cety... |
| Active Ingredient | Crotamiton |
| Dosage Form | Lotion |
| Route | Topical |
| Strength | 10% |
| Market Status | Prescription |
| Company | Summers |
| 2 of 4 | |
|---|---|
| Drug Name | Eurax |
| Active Ingredient | Crotamiton |
| Dosage Form | Lotion; Cream |
| Route | Topical |
| Strength | 10% |
| Market Status | Prescription |
| Company | Ranbaxy |
| 3 of 4 | |
|---|---|
| Drug Name | Crotan |
| PubMed Health | Crotamiton (On the skin) |
| Drug Classes | Scabicide |
| Drug Label | Eurax (crotamiton USP) is a scabicidal and antipruritic agent available as a cream or lotion for topical use only. Eurax provides 10% (w/w) of the synthetic, crotamiton USP, in a vanishing-cream or emollient-lotion base containing: carbomer-934, cety... |
| Active Ingredient | Crotamiton |
| Dosage Form | Lotion |
| Route | Topical |
| Strength | 10% |
| Market Status | Prescription |
| Company | Summers |
| 4 of 4 | |
|---|---|
| Drug Name | Eurax |
| Active Ingredient | Crotamiton |
| Dosage Form | Lotion; Cream |
| Route | Topical |
| Strength | 10% |
| Market Status | Prescription |
| Company | Ranbaxy |
Pesticides
Chemicals used to destroy pests of any sort. The concept includes fungicides (FUNGICIDES, INDUSTRIAL); INSECTICIDES; RODENTICIDES; etc. (See all compounds classified as Pesticides.)
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FDF Dossiers
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DOSAGE - CREAM;TOPICAL - 10%
USFDA APPLICATION NUMBER - 6927
DOSAGE - LOTION;TOPICAL - 10%
USFDA APPLICATION NUMBER - 9112
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52
PharmaCompass offers a list of Crotamiton 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 Crotamiton manufacturer or Crotamiton supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Crotamiton manufacturer or Crotamiton supplier.
PharmaCompass also assists you with knowing the Crotamiton API Price utilized in the formulation of products. Crotamiton API Price is not always fixed or binding as the Crotamiton Price is obtained through a variety of data sources. The Crotamiton Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Eurax manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Eurax, including repackagers and relabelers. The FDA regulates Eurax manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Eurax 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 Eurax manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Eurax supplier is an individual or a company that provides Eurax active pharmaceutical ingredient (API) or Eurax finished formulations upon request. The Eurax suppliers may include Eurax API manufacturers, exporters, distributors and traders.
click here to find a list of Eurax suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Eurax DMF (Drug Master File) is a document detailing the whole manufacturing process of Eurax active pharmaceutical ingredient (API) in detail. Different forms of Eurax DMFs exist exist since differing nations have different regulations, such as Eurax USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Eurax DMF submitted to regulatory agencies in the US is known as a USDMF. Eurax USDMF includes data on Eurax's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Eurax USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Eurax 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 Eurax Drug Master File in Japan (Eurax JDMF) empowers Eurax 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 Eurax JDMF during the approval evaluation for pharmaceutical products. At the time of Eurax 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 Eurax 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 Eurax Drug Master File in Korea (Eurax KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Eurax. The MFDS reviews the Eurax KDMF as part of the drug registration process and uses the information provided in the Eurax KDMF to evaluate the safety and efficacy of the drug.
After submitting a Eurax 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 Eurax API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Eurax suppliers with KDMF on PharmaCompass.
A Eurax CEP of the European Pharmacopoeia monograph is often referred to as a Eurax Certificate of Suitability (COS). The purpose of a Eurax CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Eurax EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Eurax to their clients by showing that a Eurax CEP has been issued for it. The manufacturer submits a Eurax CEP (COS) as part of the market authorization procedure, and it takes on the role of a Eurax CEP holder for the record. Additionally, the data presented in the Eurax CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Eurax DMF.
A Eurax CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Eurax 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 Eurax suppliers with CEP (COS) on PharmaCompass.
A Eurax written confirmation (Eurax WC) is an official document issued by a regulatory agency to a Eurax manufacturer, verifying that the manufacturing facility of a Eurax active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Eurax APIs or Eurax finished pharmaceutical products to another nation, regulatory agencies frequently require a Eurax WC (written confirmation) as part of the regulatory process.
click here to find a list of Eurax suppliers with Written Confirmation (WC) on PharmaCompass.
Eurax 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 Eurax 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 Eurax GMP manufacturer or Eurax GMP API supplier for your needs.
A Eurax CoA (Certificate of Analysis) is a formal document that attests to Eurax's compliance with Eurax specifications and serves as a tool for batch-level quality control.
Eurax CoA mostly includes findings from lab analyses of a specific batch. For each Eurax 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.
Eurax may be tested according to a variety of international standards, such as European Pharmacopoeia (Eurax EP), Eurax JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Eurax USP).
