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1. 2,14-di-(demethoxy)-2-glucosidoxy-14- Methylthiocolchicine
2. Coltramyl
3. Miorel
4. Myoplge
5. Thiocolchicoside
1. Coltramyl
2. Thiocolchicine Glycoside
3. Coltrax
4. Miorel
5. N-[1,2-dimethoxy-10-methylsulfanyl-9-oxo-3-[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxy-6,7-dihydro-5h-benzo[a]heptalen-7-yl]acetamide
6. Nsc624673
7. 2-demethoxy-2-glucosidoxythiocolchicine
8. Nsc-147755
9. Thiocolchicoside-d3
10. Prestwick_875
11. Prestwick0_000539
12. Prestwick1_000539
13. Prestwick2_000539
14. Prestwick3_000539
15. Bspbio_000557
16. Mls002153865
17. 602-41-5 (unlabeled)
18. Schembl719194
19. Spbio_002478
20. Bpbio1_000613
21. Chembl1705373
22. Chebi:91529
23. Hms1569l19
24. Hms2096l19
25. Hms2234k08
26. Bdbm50248250
27. N-[1,2-dimethoxy-10-methylsulfanyl-9-oxo-3-[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6,7-dihydro-5h-benzo[a]heptalen-7-yl]acetamide
28. Smr001233221
29. Sr-01000841233
30. Q1165293
31. Sr-01000841233-2
32. Brd-a11605036-001-03-2
33. N-(3-(hexopyranosyloxy)-1,2-dimethoxy-10-(methylthio)-9-oxo-5,6,7,9-tetrahydrobenzo[a]heptalen-7-yl)acetamide
| Molecular Weight | 563.6 g/mol |
|---|---|
| Molecular Formula | C27H33NO10S |
| XLogP3 | -0.4 |
| Hydrogen Bond Donor Count | 5 |
| Hydrogen Bond Acceptor Count | 11 |
| Rotatable Bond Count | 7 |
| Exact Mass | 563.18251742 g/mol |
| Monoisotopic Mass | 563.18251742 g/mol |
| Topological Polar Surface Area | 189 Ų |
| Heavy Atom Count | 39 |
| Formal Charge | 0 |
| Complexity | 1010 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 5 |
| Undefined Atom Stereocenter Count | 1 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
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PharmaCompass offers a list of Thiocolchicoside 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 Thiocolchicoside manufacturer or Thiocolchicoside supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Thiocolchicoside manufacturer or Thiocolchicoside supplier.
PharmaCompass also assists you with knowing the Thiocolchicoside API Price utilized in the formulation of products. Thiocolchicoside API Price is not always fixed or binding as the Thiocolchicoside Price is obtained through a variety of data sources. The Thiocolchicoside Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Musco-ril manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Musco-ril, including repackagers and relabelers. The FDA regulates Musco-ril manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Musco-ril 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 Musco-ril manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Musco-ril supplier is an individual or a company that provides Musco-ril active pharmaceutical ingredient (API) or Musco-ril finished formulations upon request. The Musco-ril suppliers may include Musco-ril API manufacturers, exporters, distributors and traders.
click here to find a list of Musco-ril suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Musco-ril DMF (Drug Master File) is a document detailing the whole manufacturing process of Musco-ril active pharmaceutical ingredient (API) in detail. Different forms of Musco-ril DMFs exist exist since differing nations have different regulations, such as Musco-ril USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Musco-ril DMF submitted to regulatory agencies in the US is known as a USDMF. Musco-ril USDMF includes data on Musco-ril's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Musco-ril USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Musco-ril suppliers with USDMF on PharmaCompass.
A Musco-ril CEP of the European Pharmacopoeia monograph is often referred to as a Musco-ril Certificate of Suitability (COS). The purpose of a Musco-ril CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Musco-ril EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Musco-ril to their clients by showing that a Musco-ril CEP has been issued for it. The manufacturer submits a Musco-ril CEP (COS) as part of the market authorization procedure, and it takes on the role of a Musco-ril CEP holder for the record. Additionally, the data presented in the Musco-ril CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Musco-ril DMF.
A Musco-ril CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Musco-ril 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 Musco-ril suppliers with CEP (COS) on PharmaCompass.
A Musco-ril written confirmation (Musco-ril WC) is an official document issued by a regulatory agency to a Musco-ril manufacturer, verifying that the manufacturing facility of a Musco-ril active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Musco-ril APIs or Musco-ril finished pharmaceutical products to another nation, regulatory agencies frequently require a Musco-ril WC (written confirmation) as part of the regulatory process.
click here to find a list of Musco-ril suppliers with Written Confirmation (WC) on PharmaCompass.
Musco-ril 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 Musco-ril 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 Musco-ril GMP manufacturer or Musco-ril GMP API supplier for your needs.
A Musco-ril CoA (Certificate of Analysis) is a formal document that attests to Musco-ril's compliance with Musco-ril specifications and serves as a tool for batch-level quality control.
Musco-ril CoA mostly includes findings from lab analyses of a specific batch. For each Musco-ril 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.
Musco-ril may be tested according to a variety of international standards, such as European Pharmacopoeia (Musco-ril EP), Musco-ril JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Musco-ril USP).
