Synopsis
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CEP/COS
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JDMF
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EU WC
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KDMF
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VMF
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Listed Suppliers
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FDF
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Europe
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Canada
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Australia
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South Africa
DRUG PRODUCT COMPOSITIONS
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US Patents
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US Exclusivities
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Health Canada Patents
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Data Compilation #PharmaFlow
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Stock Recap #PipelineProspector
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Weekly News Recap #Phispers
US Medicaid
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Annual Reports
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Finished Drug Prices
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1. Ammonium Monofluorophosphate
2. Calcium Fluorophosphate
3. Calcium Monofluorophosphate
4. Fluorophosphate
5. Fluorophosphate Hydrate, Calcium Salt
6. Fluorophosphate, Barium Salt
7. Fluorophosphate, Calcium Salt
8. Fluorophosphate, Diammonium Salt
9. Fluorophosphate, Disodium Salt
10. Fluorophosphate, Monoammonium Salt
11. Fluorophosphate, Potassium Salt
12. Fluorophosphate, Sodium Salt
13. Fluorophosphate, Tin Salt
14. Fluorophosphate, Vanadium Salt
15. Mono-tridin
16. Monofluorophosphate
17. Na-mfp
1. 10163-15-2
2. Sodium Fluorophosphate
3. Disodium Monofluorophosphate
4. Disodium Fluorophosphate
5. Sodium Phosphorofluoridate
6. 7631-97-2
7. Phosphorofluoridic Acid, Disodium Salt
8. Disodium Phosphorofluoridate
9. Acorea
10. Sodium Fluorophosphate (na2po3f)
11. Phosphorofluoridic Acid, Sodium Salt
12. C810jcz56q
13. 12331-99-6
14. Disodium;fluoro-dioxido-oxo-lambda5-phosphane
15. Chebi:86431
16. Sodium Monofluorophosphate [usp]
17. Nsc-248
18. Phosphorofluoridic Acid, Disodium Salt (8ci,9ci)
19. Mfcd00014248
20. Extra-strength Aim
21. Sodium Monofluorophosphate (usp)
22. Sodium Monofluorophosphate (inci)
23. Sodium Monofluorophosphate [inci]
24. Ccris 9129
25. Nsc 248
26. Disodiummonofluorophosphate
27. Einecs 233-433-0
28. Colgate Anticavity Toothpaste
29. Unii-c810jcz56q
30. F-o3-p.2na
31. Ai3-16931
32. Fluorophosphoric Acid, Sodium Salt
33. Sodium Fluophosphate
34. Einecs 231-552-2
35. Phoskadent Na211
36. Sodiumphosphorofluoridate
37. Sodium Phosphorofluridate
38. Aim (tn)
39. Disodium Phosphofluoridate
40. Disodiumphosphorofluoridate
41. Disodium Fluoro-dioxido-oxo-$l^{5}-phosphane
42. Ec 233-433-0
43. Na2-p-f-o3
44. Sodium Fluorophosphate, 95%
45. Sodiumfluorophosphate(na2po3f)
46. Sodium Monofluorphosphate
47. Phosphorofluoridicacid,sodiumsalt
48. Sodium Monofluorophosphate, Usp
49. Chembl1908359
50. F-h2-o3-p
51. Dtxsid70872554
52. Hms3264b14
53. Phosphorofluoridic Acid,sodium Salt
54. Phosphorofluoridicacid, Sodium Salt
55. Amy37031
56. Fluoridophosphoric Acid Disodium Salt
57. Phosphorofluoridic Acid Disodium Salt
58. S4013
59. Akos015916166
60. Akos015960447
61. Ccg-213673
62. Db09484
63. Sodium Fluorophosphate [who-dd]
64. Superlist Name Sodium Monofluorophosphate
65. Sodium Monofluorophosphate [mart.]
66. Sy061225
67. Sodium Monofluorophosphate [usp-rs]
68. Phosphorofluoridic Acid, Disodium Salt Smfp
69. Disodium;fluoro-dioxido-oxo-$l^{5-phosphane
70. Ft-0688148
71. Phosphorofluoridic Acid, Sodium Salt (1:?)
72. D05864
73. Sodium Monofluorophosphate [orange Book]
74. A838673
75. Sodium Monofluorophosphate [usp Monograph]
76. Q3498849
Molecular Weight | 143.950 g/mol |
---|---|
Molecular Formula | FNa2O3P |
Hydrogen Bond Donor Count | 0 |
Hydrogen Bond Acceptor Count | 4 |
Rotatable Bond Count | 0 |
Exact Mass | 143.93644758 g/mol |
Monoisotopic Mass | 143.93644758 g/mol |
Topological Polar Surface Area | 63.2 Ų |
Heavy Atom Count | 7 |
Formal Charge | 0 |
Complexity | 49.8 |
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 | 3 |
Sodium monofluorophosphate is indicated for the treatment of cavities
Cariostatic Agents
Substances that inhibit or arrest DENTAL CARIES formation. (Boucher's Clinical Dental Terminology, 4th ed) (See all compounds classified as Cariostatic Agents.)
A - Alimentary tract and metabolism
A01 - Stomatological preparations
A01A - Stomatological preparations
A01AA - Caries prophylactic agents
A01AA02 - Sodium monofluorophosphate
A - Alimentary tract and metabolism
A12 - Mineral supplements
A12C - Other mineral supplements
A12CD - Fluoride
A12CD02 - Sodium monofluorophosphate
API Imports and Exports
Importing Country | Total Quantity (KGS) |
Average Price (USD/KGS) |
Number of Transactions |
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REF. STANDARDS & IMPURITIES
ABOUT THIS PAGE
A Fluorophosphate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fluorophosphate, including repackagers and relabelers. The FDA regulates Fluorophosphate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fluorophosphate 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 Fluorophosphate supplier is an individual or a company that provides Fluorophosphate active pharmaceutical ingredient (API) or Fluorophosphate finished formulations upon request. The Fluorophosphate suppliers may include Fluorophosphate API manufacturers, exporters, distributors and traders.
click here to find a list of Fluorophosphate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Fluorophosphate DMF (Drug Master File) is a document detailing the whole manufacturing process of Fluorophosphate active pharmaceutical ingredient (API) in detail. Different forms of Fluorophosphate DMFs exist exist since differing nations have different regulations, such as Fluorophosphate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Fluorophosphate DMF submitted to regulatory agencies in the US is known as a USDMF. Fluorophosphate USDMF includes data on Fluorophosphate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Fluorophosphate USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Fluorophosphate suppliers with USDMF 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 Fluorophosphate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Fluorophosphate 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 Fluorophosphate 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 Fluorophosphate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Fluorophosphate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Fluorophosphate suppliers with NDC on PharmaCompass.
Fluorophosphate 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 Fluorophosphate 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 Fluorophosphate GMP manufacturer or Fluorophosphate GMP API supplier for your needs.
A Fluorophosphate CoA (Certificate of Analysis) is a formal document that attests to Fluorophosphate's compliance with Fluorophosphate specifications and serves as a tool for batch-level quality control.
Fluorophosphate CoA mostly includes findings from lab analyses of a specific batch. For each Fluorophosphate 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.
Fluorophosphate may be tested according to a variety of international standards, such as European Pharmacopoeia (Fluorophosphate EP), Fluorophosphate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Fluorophosphate USP).
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