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1. 31121-93-4
2. Ibuprofen Sodium Salt
3. Sodium Ibuprofen
4. Sodium 2-(4-isobutylphenyl)propionate
5. Sodium 2-[4-(2-methylpropyl)phenyl]propanoate
6. Ibuprofen Sodium Anhydrous
7. P-isobutylhydratropic Acid Sodium Salt
8. Sodium 2-(4-isobutylphenyl)propanoate
9. Ibuprofen (sodium)
10. Sodium;2-[4-(2-methylpropyl)phenyl]propanoate
11. O0pj4uz01u
12. Ibuprofensodiumsalt
13. Einecs 250-477-6
14. Unii-o0pj4uz01u
15. Esprenit (tn)
16. Sodium Ibuprofen Salt
17. Hydratropic Acid, P-isobutyl-, Sodium Salt
18. Benzeneacetic Acid, Alpha-methyl-4-(2-methylpropyl)-, Sodium Salt
19. Schembl139269
20. Chembl1241153
21. Dtxsid4040501
22. Smsf0005424
23. Hy-78131c
24. Sodium2-(4-isobutylphenyl)propanoate
25. Akos015994627
26. Cb08098
27. Hs-0087
28. Sodium 2-(4'-isobutylphenyl)propionate
29. 5264-06-2
30. Bim-0005680.p001
31. Cs-0031024
32. 2-(p-isobutylphenyl)propionic Acid Sodium Salt
33. D08059
34. ((c)i)-ibuprofen-d3, Sodium Salt (
35. A-methyl-d3)
36. W-110791
37. Q27285172
38. Benzeneacetic Acid, .alpha.-methyl-4-(2-methylpropyl)-, Sodium Salt (1:1)
39. Benzeneacetic Acid, .alpha.-methyl-4-(2-methylpropyl)-,sodium Salt
Molecular Weight | 228.26 g/mol |
---|---|
Molecular Formula | C13H17NaO2 |
Hydrogen Bond Donor Count | 0 |
Hydrogen Bond Acceptor Count | 2 |
Rotatable Bond Count | 4 |
Exact Mass | 228.11262406 g/mol |
Monoisotopic Mass | 228.11262406 g/mol |
Topological Polar Surface Area | 40.1 Ų |
Heavy Atom Count | 16 |
Formal Charge | 0 |
Complexity | 208 |
Isotope Atom Count | 0 |
Defined Atom Stereocenter Count | 0 |
Undefined Atom Stereocenter Count | 1 |
Defined Bond Stereocenter Count | 0 |
Undefined Bond Stereocenter Count | 0 |
Covalently Bonded Unit Count | 2 |
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ABOUT THIS PAGE
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PharmaCompass offers a list of Ibuprofen Sodium 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 Ibuprofen Sodium manufacturer or Ibuprofen Sodium supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ibuprofen Sodium manufacturer or Ibuprofen Sodium supplier.
PharmaCompass also assists you with knowing the Ibuprofen Sodium API Price utilized in the formulation of products. Ibuprofen Sodium API Price is not always fixed or binding as the Ibuprofen Sodium Price is obtained through a variety of data sources. The Ibuprofen Sodium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Ibuprofen Sodium Dihydrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ibuprofen Sodium Dihydrate, including repackagers and relabelers. The FDA regulates Ibuprofen Sodium Dihydrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ibuprofen Sodium Dihydrate 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 Ibuprofen Sodium Dihydrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ibuprofen Sodium Dihydrate supplier is an individual or a company that provides Ibuprofen Sodium Dihydrate active pharmaceutical ingredient (API) or Ibuprofen Sodium Dihydrate finished formulations upon request. The Ibuprofen Sodium Dihydrate suppliers may include Ibuprofen Sodium Dihydrate API manufacturers, exporters, distributors and traders.
click here to find a list of Ibuprofen Sodium Dihydrate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Ibuprofen Sodium Dihydrate DMF (Drug Master File) is a document detailing the whole manufacturing process of Ibuprofen Sodium Dihydrate active pharmaceutical ingredient (API) in detail. Different forms of Ibuprofen Sodium Dihydrate DMFs exist exist since differing nations have different regulations, such as Ibuprofen Sodium Dihydrate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Ibuprofen Sodium Dihydrate DMF submitted to regulatory agencies in the US is known as a USDMF. Ibuprofen Sodium Dihydrate USDMF includes data on Ibuprofen Sodium Dihydrate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Ibuprofen Sodium Dihydrate USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Ibuprofen Sodium Dihydrate suppliers with USDMF 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 Ibuprofen Sodium Dihydrate Drug Master File in Korea (Ibuprofen Sodium Dihydrate KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Ibuprofen Sodium Dihydrate. The MFDS reviews the Ibuprofen Sodium Dihydrate KDMF as part of the drug registration process and uses the information provided in the Ibuprofen Sodium Dihydrate KDMF to evaluate the safety and efficacy of the drug.
After submitting a Ibuprofen Sodium Dihydrate 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 Ibuprofen Sodium Dihydrate API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Ibuprofen Sodium Dihydrate suppliers with KDMF on PharmaCompass.
A Ibuprofen Sodium Dihydrate written confirmation (Ibuprofen Sodium Dihydrate WC) is an official document issued by a regulatory agency to a Ibuprofen Sodium Dihydrate manufacturer, verifying that the manufacturing facility of a Ibuprofen Sodium Dihydrate active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Ibuprofen Sodium Dihydrate APIs or Ibuprofen Sodium Dihydrate finished pharmaceutical products to another nation, regulatory agencies frequently require a Ibuprofen Sodium Dihydrate WC (written confirmation) as part of the regulatory process.
click here to find a list of Ibuprofen Sodium Dihydrate suppliers with Written Confirmation (WC) 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 Ibuprofen Sodium Dihydrate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Ibuprofen Sodium Dihydrate 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 Ibuprofen Sodium Dihydrate 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 Ibuprofen Sodium Dihydrate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Ibuprofen Sodium Dihydrate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Ibuprofen Sodium Dihydrate suppliers with NDC on PharmaCompass.
Ibuprofen Sodium Dihydrate 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 Ibuprofen Sodium Dihydrate 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 Ibuprofen Sodium Dihydrate GMP manufacturer or Ibuprofen Sodium Dihydrate GMP API supplier for your needs.
A Ibuprofen Sodium Dihydrate CoA (Certificate of Analysis) is a formal document that attests to Ibuprofen Sodium Dihydrate's compliance with Ibuprofen Sodium Dihydrate specifications and serves as a tool for batch-level quality control.
Ibuprofen Sodium Dihydrate CoA mostly includes findings from lab analyses of a specific batch. For each Ibuprofen Sodium Dihydrate 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.
Ibuprofen Sodium Dihydrate may be tested according to a variety of international standards, such as European Pharmacopoeia (Ibuprofen Sodium Dihydrate EP), Ibuprofen Sodium Dihydrate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Ibuprofen Sodium Dihydrate USP).