Synopsis
Synopsis
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USDMF
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KDMF
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NDC API
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Europe
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Canada
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Australia
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Listed Dossiers
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USP
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JP
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1. Soothe
2. Crospovidone
3. Polyplasdone
4. Polyvidonum
5. Agrimer
6. Disadine
7. Refresh
8. Toxobin
9. Povidone(usan)
10. Tears Plus
11. Aldacol Q
12. Kollidon Cl
13. Kollidin Clm
14. Plasdone 4
15. Luviskol K30
16. Luviskol K90
17. Polyclar A. T
18. Polyvinyl Pyrrolidone
19. Polividone [dcit]
20. K25 (polymer)
21. K30 (polymer)
22. K60 (polymer)
23. K115 (polyamide)
24. Polyvinylpolypyrrolidone
25. Agent At 717
26. Plasdone K-26/28
27. Povidone, Ban, Usan
28. Pvp10_sial
29. Pvp40_sial
30. Povidone [usan:inn:ban]
31. Pvp-k 15
32. Poly(1-ethenyl-2-pyrrolidinone)
33. Chebi:185135
34. Polyvinylpyrrolidone, Cross-linked
35. K 25 (van)
36. K 30 (van)
37. K 60 (van)
38. 1-ethenyl-2-pyrrolidinone (9ci)
39. Tolpovidone I 131 [usan:inn]
40. 1-vinyl-2-pyrrolidinone Homopolymer
41. 1-ethenyl-2-pyrrolidinone Homopolymer
42. 2-pyrrolidinone, 1-vinyl-, Polymers
43. 1-ethenyl-2-pyrrolidinone, Homopolymer
44. 2-pyrrolidinone, 1-ethenyl, Homopolymer
45. 1-(1,2-diphosphanylethyl)pyrrolidin-2-one
46. 1-ethenyl-2-pyrrolidinone Homopolymer, 9ci
47. 1-[1,2-bis(phosphanyl)ethyl]pyrrolidin-2-one
48. 1-vinyl-2-pyrrolidinone Cross-linked Insoluble Polymer
| Molecular Weight | 177.12 g/mol |
|---|---|
| Molecular Formula | C6H13NOP2 |
| XLogP3 | -0.7 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 2 |
| Exact Mass | 177.04723803 g/mol |
| Monoisotopic Mass | 177.04723803 g/mol |
| Topological Polar Surface Area | 20.3 Ų |
| Heavy Atom Count | 10 |
| Formal Charge | 0 |
| Complexity | 140 |
| 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 | 1 |
A - Alimentary tract and metabolism
A07 - Antidiarrheals, intestinal antiinflammatory/antiinfective agents
A07B - Intestinal adsorbents
A07BC - Other intestinal adsorbents
A07BC03 - Crospovidone
ABOUT THIS PAGE
A Soothe manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Soothe, including repackagers and relabelers. The FDA regulates Soothe manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Soothe 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 Soothe supplier is an individual or a company that provides Soothe active pharmaceutical ingredient (API) or Soothe finished formulations upon request. The Soothe suppliers may include Soothe API manufacturers, exporters, distributors and traders.
click here to find a list of Soothe suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Soothe CEP of the European Pharmacopoeia monograph is often referred to as a Soothe Certificate of Suitability (COS). The purpose of a Soothe CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Soothe EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Soothe to their clients by showing that a Soothe CEP has been issued for it. The manufacturer submits a Soothe CEP (COS) as part of the market authorization procedure, and it takes on the role of a Soothe CEP holder for the record. Additionally, the data presented in the Soothe CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Soothe DMF.
A Soothe CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Soothe CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of Soothe suppliers with CEP (COS) on PharmaCompass.
Soothe 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 Soothe 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 Soothe GMP manufacturer or Soothe GMP API supplier for your needs.
A Soothe CoA (Certificate of Analysis) is a formal document that attests to Soothe's compliance with Soothe specifications and serves as a tool for batch-level quality control.
Soothe CoA mostly includes findings from lab analyses of a specific batch. For each Soothe 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.
Soothe may be tested according to a variety of international standards, such as European Pharmacopoeia (Soothe EP), Soothe JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Soothe USP).
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