Synopsis
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NDC API
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1. Ospolot
2. P-(tetrahydro-2h-1,2-thiazin-2-yl)benzenesulfonamide, S,s-dioxide
3. Sulthiame
4. Sultiam
1. Sulthiame
2. 61-56-3
3. Ospolot
4. Trolone
5. Sultiam
6. Sulphenyltame
7. Sulthiamine
8. Conadil
9. Contravul
10. Riker 594
11. Sultiamum
12. Elisal
13. Bayer A-168
14. Sulthiame [usan]
15. 4-(1,1-dioxothiazinan-2-yl)benzenesulfonamide
16. 4-(1,1-dioxido-1,2-thiazinan-2-yl)benzenesulfonamide
17. Sultiame [inn]
18. Rp-10284
19. P-(tetrahydro-2h-1,2-thiazin-2-yl)benzenesulfonamide, S,s-dioxide
20. Benzenesulfonamide, 4-(tetrahydro-2h-1,2-thiazin-2-yl)-, S,s-dioxide
21. R-594
22. Riker-594
23. Chembl328560
24. 2-(p-sulfamoylphenyl)-tetrahydro-2h-1,2-thiazine 1,1-dioxide
25. Chebi:32171
26. 2h-1,2-thiazine, Tetrahydro-2-(p-sulfamoylphenyl)-, 1,1-dioxide
27. I00q766cz2
28. Sulthiame (usan)
29. Benzenesulfonamide, P-(tetrahydro-2h-1,2-thiazin-2-yl)-, Dioxide
30. Sultiamo
31. Sultiamum [inn-latin]
32. Sultiamo [inn-spanish]
33. Einecs 200-511-0
34. Brn 1222219
35. Rp 10284
36. Unii-i00q766cz2
37. Sulthiame, 2
38. Sulthiame (slt)
39. 2-(4-sulfamoylphenyl)-1,2-thiazixan 1,1-dioxid
40. Ospolot (tn)
41. Sultiame (jp17)
42. 2q1q
43. Sulthiame [mi]
44. Sultiame [jan]
45. Dsstox_cid_3626
46. Sultiame [mart.]
47. Sultiame [who-dd]
48. Dsstox_rid_97552
49. Dsstox_gsid_23626
50. Oprea1_326703
51. Schembl38898
52. Zinc2119
53. Dtxsid4023626
54. Bdbm26999
55. Hms3746a19
56. Bcp30158
57. Tox21_113683
58. 4-(tetrahydro-2h-1,2-thiazin-2-yl)benzenesulfonamide S,s-dioxide
59. Cs-7868
60. Db08329
61. Cas-61-56-3
62. Sultiame 100 Microg/ml In Acetonitrile
63. Ncgc00249907-01
64. As-83082
65. Hy-108316
66. Ft-0674777
67. D01787
68. Q2364943
69. 4-(1,1-dioxido-1,2-thiazinan-2-yl)benzenesulfonamide #
70. 4-(1,1-dioxo-1i>>6-[1,2]thiazinan-2-yl)-benzenesulfonamide
71. P-(tetrahydro-2h-1,2-thiazin-2-yl)benzenesulfonamide Dioxide
72. 4-(1,1-dioxo-1$l^{6},2-thiazinan-2-yl)benzene-1-sulfonamide
73. 4-(tetrahydro-1,1-dioxido-2h-1,2-thiazin-2-yl)benzenesulfonamide
74. 4-(tetrahydro-2h-1,2-thiazin-2-yl)benzenesulfonamide, S,s-dioxide
75. Osp
Molecular Weight | 290.4 g/mol |
---|---|
Molecular Formula | C10H14N2O4S2 |
XLogP3 | 0.1 |
Hydrogen Bond Donor Count | 1 |
Hydrogen Bond Acceptor Count | 6 |
Rotatable Bond Count | 2 |
Exact Mass | 290.03949928 g/mol |
Monoisotopic Mass | 290.03949928 g/mol |
Topological Polar Surface Area | 114 Ų |
Heavy Atom Count | 18 |
Formal Charge | 0 |
Complexity | 481 |
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 |
Anticonvulsants
Drugs used to prevent SEIZURES or reduce their severity. (See all compounds classified as Anticonvulsants.)
N - Nervous system
N03 - Antiepileptics
N03A - Antiepileptics
N03AX - Other antiepileptics
N03AX03 - Sultiame
About the Company : Arevipharma GmbH is a modern manufacturer of active pharmaceutical ingredients and intermediates with more than 140 years of expertise. Our customers are generic and research-based...
Regulatory Info :
Registration Country : Switzerland
Brand Name : Ospolot
Dosage Form : Film-Coated Tablets
Dosage Strength : 200mg
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Regulatory Info :
Registration Country : Switzerland
Regulatory Info :
Registration Country : Switzerland
Brand Name : Ospolot
Dosage Form : Film-Coated Tablets
Dosage Strength : 50mg
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Regulatory Info :
Registration Country : Switzerland
Regulatory Info :
Registration Country : Spain
Brand Name :
Dosage Form : Film Coated Tablet
Dosage Strength : 50MG
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Regulatory Info :
Registration Country : Spain
Regulatory Info :
Registration Country : Spain
Brand Name :
Dosage Form : Film Coated Tablet
Dosage Strength : 100MG
Packaging :
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Regulatory Info :
Registration Country : Spain
Regulatory Info :
Registration Country : Spain
Brand Name :
Dosage Form : Film Coated Tablet
Dosage Strength : 200MG
Packaging :
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Regulatory Info :
Registration Country : Spain
Regulatory Info :
Registration Country : Australia
Brand Name : Ospolot
Dosage Form : tablet
Dosage Strength : 50 mg
Packaging : 200
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Australia
Regulatory Info :
Registration Country : Australia
Brand Name : Ospolot
Dosage Form : tablet
Dosage Strength : 200 mg
Packaging : 200
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Australia
Regulatory Info :
Registration Country : Australia
Brand Name : Ospolot
Dosage Form : tablet
Dosage Strength : 50 mg
Packaging : 200
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Australia
Regulatory Info :
Registration Country : Australia
Brand Name : Ospolot
Dosage Form : tablet
Dosage Strength : 200 mg
Packaging : 200
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Australia
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ABOUT THIS PAGE
A Sulthiame manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sulthiame, including repackagers and relabelers. The FDA regulates Sulthiame manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sulthiame 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 Sulthiame manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sulthiame supplier is an individual or a company that provides Sulthiame active pharmaceutical ingredient (API) or Sulthiame finished formulations upon request. The Sulthiame suppliers may include Sulthiame API manufacturers, exporters, distributors and traders.
click here to find a list of Sulthiame suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
Sulthiame 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 Sulthiame 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 Sulthiame GMP manufacturer or Sulthiame GMP API supplier for your needs.
A Sulthiame CoA (Certificate of Analysis) is a formal document that attests to Sulthiame's compliance with Sulthiame specifications and serves as a tool for batch-level quality control.
Sulthiame CoA mostly includes findings from lab analyses of a specific batch. For each Sulthiame 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.
Sulthiame may be tested according to a variety of international standards, such as European Pharmacopoeia (Sulthiame EP), Sulthiame JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Sulthiame USP).
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