Synopsis
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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NDC API
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VMF
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Listed Suppliers
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EDQM
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USP
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JP
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Others
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FDF Dossiers
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FDA Orange Book
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Europe
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Canada
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Australia
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South Africa
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Listed Dossiers
DRUG PRODUCT COMPOSITIONS
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US Patents
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US Exclusivities
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Health Canada Patents
US Medicaid
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Regulatory FDF Prices
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API
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FDF
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Data Compilation #PharmaFlow
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1. 555-06-6
2. Aminobenzoate Sodium
3. 4-aminobenzoic Acid Sodium Salt
4. Sodium P-aminobenzoate
5. Sodium Aminobenzoate
6. Antergyl
7. Benzoic Acid, 4-amino-, Monosodium Salt
8. Sodium;4-aminobenzoate
9. Sodium Para-aminobenzoate
10. Benzoic Acid, P-amino-, Monosodium Salt
11. 4-aminobenzoic Acid Sodium
12. 75ui7quz5j
13. 4-aminobenzoic Acid, Sodium Salt
14. Pabavit
15. Monosodium 4-aminobenzoate
16. Chembl1762658
17. Sodium4-aminobenzoate
18. P-aminobenzoic Acid, Sodium Salt
19. Einecs 209-080-3
20. Unii-75ui7quz5j
21. Ai3-16691
22. Mfcd00064395
23. Benzoic Acid, 4-amino-, Sodium Salt
24. Sodium 4-azanylbenzoate
25. Ec 209-080-3
26. Aminobenzoate Sodium (usp)
27. Schembl587865
28. 4-aminobenzoic Acid Sodium Sal
29. Dtxsid8060296
30. 4-aminobenzoicacidsodiumsalt
31. Benzoic Acid, P-amino-, Sodium Salt
32. Sodium Aminobenzoate [mart.]
33. Aminobenzoate Sodium [usp-rs]
34. Sodium Aminobenzoate [who-dd]
35. Akos003051697
36. Akos015888388
37. Akos015950610
38. Akos024272189
39. 54287-22-8
40. As-57673
41. Aminobenzoate Sodium [usp Impurity]
42. Aminobenzoate Sodium [usp Monograph]
43. Db-052748
44. A0276
45. Ft-0617562
46. Benzoic Acid, 4-amino-, Sodium Salt (1:1)
47. D02907
48. O12079
49. A830682
50. W-105558
51. Q27266411
| Molecular Weight | 159.12 g/mol |
|---|---|
| Molecular Formula | C7H6NNaO2 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 1 |
| Exact Mass | 159.02962272 g/mol |
| Monoisotopic Mass | 159.02962272 g/mol |
| Topological Polar Surface Area | 66.2 Ų |
| Heavy Atom Count | 11 |
| Formal Charge | 0 |
| Complexity | 132 |
| 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
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PharmaCompass offers a list of Sodium 4-Aminobenzoate 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 Sodium 4-Aminobenzoate manufacturer or Sodium 4-Aminobenzoate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Sodium 4-Aminobenzoate manufacturer or Sodium 4-Aminobenzoate supplier.
PharmaCompass also assists you with knowing the Sodium 4-Aminobenzoate API Price utilized in the formulation of products. Sodium 4-Aminobenzoate API Price is not always fixed or binding as the Sodium 4-Aminobenzoate Price is obtained through a variety of data sources. The Sodium 4-Aminobenzoate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A potassium sunbrella manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of potassium sunbrella, including repackagers and relabelers. The FDA regulates potassium sunbrella manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. potassium sunbrella 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 potassium sunbrella supplier is an individual or a company that provides potassium sunbrella active pharmaceutical ingredient (API) or potassium sunbrella finished formulations upon request. The potassium sunbrella suppliers may include potassium sunbrella API manufacturers, exporters, distributors and traders.
click here to find a list of potassium sunbrella suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A potassium sunbrella DMF (Drug Master File) is a document detailing the whole manufacturing process of potassium sunbrella active pharmaceutical ingredient (API) in detail. Different forms of potassium sunbrella DMFs exist exist since differing nations have different regulations, such as potassium sunbrella USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A potassium sunbrella DMF submitted to regulatory agencies in the US is known as a USDMF. potassium sunbrella USDMF includes data on potassium sunbrella's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The potassium sunbrella USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of potassium sunbrella suppliers with USDMF on PharmaCompass.
potassium sunbrella 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 potassium sunbrella 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 potassium sunbrella GMP manufacturer or potassium sunbrella GMP API supplier for your needs.
A potassium sunbrella CoA (Certificate of Analysis) is a formal document that attests to potassium sunbrella's compliance with potassium sunbrella specifications and serves as a tool for batch-level quality control.
potassium sunbrella CoA mostly includes findings from lab analyses of a specific batch. For each potassium sunbrella 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.
potassium sunbrella may be tested according to a variety of international standards, such as European Pharmacopoeia (potassium sunbrella EP), potassium sunbrella JP (Japanese Pharmacopeia) and the US Pharmacopoeia (potassium sunbrella USP).