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1. 4955-90-2
2. Sodium 2,5-dihydroxybenzoate
3. Gentisic Acid Sodium Salt
4. Gentalpin
5. Gentasol
6. Gentidol
7. Gentinatre
8. Gentisan
9. Gentisod
10. Legential
11. Nagentis
12. Casate
13. Gabail
14. Nagent
15. Casate Sodium
16. Gensalate Sodium
17. Sodium;2,5-dihydroxybenzoate
18. Benzoic Acid, 2,5-dihydroxy-, Monosodium Salt
19. Sodium Gentisate [inn]
20. 5-hydroxysalicylate Sodium
21. Gentisate Sodium
22. Gentisic Acid Sodium
23. Sodium Gentisate Anhydrous
24. Gentisic Acid, Monosodium Salt
25. 2,5-dihydroxybenzoic Acid Sodium Salt
26. Dx2pud5h82
27. Nsc-8512
28. 2,5-dihydroxybenzoic Acid Sodium
29. Gentasol (van)
30. Natrii Gentisas
31. Gentisato Sodico
32. Gentisato Sodico [dcit]
33. Gentisate De Sodium
34. Natrii Gentisas [inn-latin]
35. Monosodium 2,5-dihydroxybenzoate
36. Gentisate De Sodium [inn-french]
37. Nsc 8512
38. Einecs 225-598-2
39. Resorcyclic Acid, Alpha-, Sodium Salt
40. Unii-dx2pud5h82
41. Natriumgentisat
42. Salicylic Acid, 5-hydroxy-, Sodium Salt
43. Ai3-18005
44. Benzoic Acid, 2,5-dihydroxy-, Sodium Salt
45. Sodium2,5-dihydroxybenzoate
46. Schembl453133
47. Chembl2107562
48. Dtxsid0063656
49. Chebi:189437
50. Sodium Gentisate [who-dd]
51. Amy18474
52. Ac-937
53. Sodium-2,5-dihydroxybenzoate
54. Akos015838930
55. Akos015890000
56. Akos015963333
57. Cs-w017420
58. Gentisic Acid Sodium Salt [mi]
59. 106120-03-0
60. D4893
61. Ft-0626647
62. H11049
63. A827744
64. Benzoic Acid, 2,5-dihydroxy-, Sodium Salt (1:1)
65. W-106020
66. Q27276656
67. 2,5-dihydroxybenzoic Acid Sodium Salt, 5-hydroxysalicylate Sodium
68. Sodium 2,5-dihydroxybenzoic Acid;gentisic Acid Sodium Salt Hydrate
| Molecular Weight | 176.10 g/mol |
|---|---|
| Molecular Formula | C7H5NaO4 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 1 |
| Exact Mass | 176.00855292 g/mol |
| Monoisotopic Mass | 176.00855292 g/mol |
| Topological Polar Surface Area | 80.6 Ų |
| Heavy Atom Count | 12 |
| Formal Charge | 0 |
| Complexity | 162 |
| 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 | 2 |
ABOUT THIS PAGE
A Sodium Gentisate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sodium Gentisate, including repackagers and relabelers. The FDA regulates Sodium Gentisate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sodium Gentisate API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Sodium Gentisate supplier is an individual or a company that provides Sodium Gentisate active pharmaceutical ingredient (API) or Sodium Gentisate finished formulations upon request. The Sodium Gentisate suppliers may include Sodium Gentisate API manufacturers, exporters, distributors and traders.
Sodium Gentisate 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 Sodium Gentisate 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 Sodium Gentisate GMP manufacturer or Sodium Gentisate GMP API supplier for your needs.
A Sodium Gentisate CoA (Certificate of Analysis) is a formal document that attests to Sodium Gentisate's compliance with Sodium Gentisate specifications and serves as a tool for batch-level quality control.
Sodium Gentisate CoA mostly includes findings from lab analyses of a specific batch. For each Sodium Gentisate 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.
Sodium Gentisate may be tested according to a variety of international standards, such as European Pharmacopoeia (Sodium Gentisate EP), Sodium Gentisate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Sodium Gentisate USP).
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