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1. 3-((2,3-cyclopenteno-1-pyridinium)methyl)-7-(2-syn-methoximino-2-(2-aminothiazole-4-yl)acetamido)ceph-3-em-4-carboxylate
2. Cefpirome Sulfate
3. Cefrom
4. Hr 810
5. Hr-810
6. Metran
1. 84957-29-9
2. Cefpiroma
3. Cefpiromum
4. Cefrom
5. Cefir
6. Cefpirome Sulfate
7. Hr 810
8. Hr-810 Free Base
9. Chebi:3503
10. S72q2f09hy
11. Hr-810
12. Cefpirome (inn)
13. (6r,7r)-7-[[(2z)-2-(2-amino-1,3-thiazol-4-yl)-2-methoxyiminoacetyl]amino]-3-(6,7-dihydro-5h-cyclopenta[b]pyridin-1-ium-1-ylmethyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate
14. Cefpirome Sulphate
15. Cefpirome [inn]
16. (6r,7r)-7-{[(2z)-2-(2-amino-1,3-thiazol-4-yl)-2-(methoxyimino)acetyl]amino}-3-(6,7-dihydro-5h-cyclopenta[b]pyridinium-1-ylmethyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate
17. 5h-cyclopenta[b]pyridinium,1-[[(6r,7r)-7-[[(2z)-(2-amino-4-thiazolyl)(methoxyimino)acetyl]amino]-2-carboxy-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-en-3-yl]methyl]-6,7-dihydro-, Inner Salt
18. Cefpiromum [latin]
19. Cefpiroma [spanish]
20. Cefpirome [inn:ban]
21. Ncgc00181339-01
22. Unii-s72q2f09hy
23. Broact
24. Keiten
25. Keiten, Cefpiroma
26. Cefir (tn)
27. Cefpirome [mi]
28. Cefpirome [who-dd]
29. Schembl49406
30. Mls006010792
31. Chembl65794
32. Dtxsid2048244
33. Schembl22207951
34. Akos016013926
35. Db13682
36. 1-(((6r,7r)-7-(2-(2-amino-4-thiazolyl)glyoxylamino)-2-carboxy-8-oxo-5-thia-1-azabicyclo(4.2.0)oct-2-en-3-yl)methyl)-6,7-dihydro-5h-1-pyridinium Hydroxide, Inner Salt
37. 5h-1-pyrindinium, 1-((7-(((2-amino-4-thiazolyl)(methoxyimino)acetyl)amino)-2-carboxy-8-oxo-5-thia-1-azabicyclo(4.2.0)oct-2-en-3-yl)methyl)-6,7-dihydro-, Hydroxide, Inner Salt, (6r-(6alpha,7beta(z)))-
38. Smr004701476
39. 98753-19-6
40. D07649
41. (6r,7r)-7-((2-(2-amino-4-thiazolyl)-2-methoxyiminoacetamido)-8-oxo-3-(2beta-trimethylenpyridinio)methyl)-5-thia-1-azabicyclo(4.2.0)oct-2-en-2-carboxylat
42. 1-(((6r,7r)-7-(2-(2-amino-4-thiazolyl)glyoxylamido)-2-carboxy-8-oxo-5-thia-1-azabicyclo(4.2.0)oct-2-en-3-yl)methyl)-6,7-dihydro-5h-1-pyrindinium Hydroxide, Inner Salt, 72-(z)-(o-methyloxime)
43. 1-{[(6r,7r)-2-carboxylato-7-{[(2z)-1-hydroxy-2-(2-imino-2,3-dihydro-1,3-thiazol-4-yl)-2-(methoxyimino)ethylidene]amino}-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-en-3-yl]methyl}-5h,6h,7h-cyclopenta[b]pyridin-1-ium
44. 5h-1-pyrindinium, 1-((7-(((2-amino-4-thiazolyl)(methoxyimino)acetyl)amino)-2-carboxy-8-oxo-5-thia-1-azabicyclo(4.2.0)oct-2-en-3-yl)methyl)-5,6,7,8-tetrahydro-, Hydroxide, Inner Salt, (6r-(6alpha,7beta(z)))-
45. 5h-1-pyrindinium, 1-((7-(((2-amino-4-thiazolyl)(methoxyimino)acetyl)amino)-2-carboxy-8-oxo-5-thia-1-azabicyclo(4.2.0)oct-2-en-3-yl)methyl)-6,7-dihydro-, Hydroxide, Inner Salt, (6r-(6.alpha.,7.beta.(z)))-
46. 7-{[(2z)-2-(2-amino-1,3-thiazol-4-yl)-2-(methoxyimino)acetyl]amino}-3-(6,7-dihydro-5h-cyclopenta[b]pyridinium-1-ylmethyl)-3,4-didehydrocepham-4-carboxylic Acid
| Molecular Weight | 514.6 g/mol |
|---|---|
| Molecular Formula | C22H22N6O5S2 |
| XLogP3 | 0.9 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 10 |
| Rotatable Bond Count | 6 |
| Exact Mass | 514.10931017 g/mol |
| Monoisotopic Mass | 514.10931017 g/mol |
| Topological Polar Surface Area | 208 Ų |
| Heavy Atom Count | 35 |
| Formal Charge | 0 |
| Complexity | 955 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 2 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 1 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
Anti-Bacterial Agents
Substances that inhibit the growth or reproduction of BACTERIA. (See all compounds classified as Anti-Bacterial Agents.)
J - Antiinfectives for systemic use
J01 - Antibacterials for systemic use
J01D - Other beta-lactam antibacterials
J01DE - Fourth-generation cephalosporins
J01DE02 - Cefpirome
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ABOUT THIS PAGE
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PharmaCompass offers a list of Cefpirome Sulphate 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 Cefpirome Sulphate manufacturer or Cefpirome Sulphate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Cefpirome Sulphate manufacturer or Cefpirome Sulphate supplier.
PharmaCompass also assists you with knowing the Cefpirome Sulphate API Price utilized in the formulation of products. Cefpirome Sulphate API Price is not always fixed or binding as the Cefpirome Sulphate Price is obtained through a variety of data sources. The Cefpirome Sulphate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Metran manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Metran, including repackagers and relabelers. The FDA regulates Metran manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Metran 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 Metran manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Metran supplier is an individual or a company that provides Metran active pharmaceutical ingredient (API) or Metran finished formulations upon request. The Metran suppliers may include Metran API manufacturers, exporters, distributors and traders.
click here to find a list of Metran suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Metran Drug Master File in Japan (Metran JDMF) empowers Metran API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Metran JDMF during the approval evaluation for pharmaceutical products. At the time of Metran JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Metran suppliers with JDMF 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 Metran Drug Master File in Korea (Metran KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Metran. The MFDS reviews the Metran KDMF as part of the drug registration process and uses the information provided in the Metran KDMF to evaluate the safety and efficacy of the drug.
After submitting a Metran 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 Metran API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Metran suppliers with KDMF on PharmaCompass.
A Metran written confirmation (Metran WC) is an official document issued by a regulatory agency to a Metran manufacturer, verifying that the manufacturing facility of a Metran active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Metran APIs or Metran finished pharmaceutical products to another nation, regulatory agencies frequently require a Metran WC (written confirmation) as part of the regulatory process.
click here to find a list of Metran suppliers with Written Confirmation (WC) on PharmaCompass.
Metran 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 Metran 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 Metran GMP manufacturer or Metran GMP API supplier for your needs.
A Metran CoA (Certificate of Analysis) is a formal document that attests to Metran's compliance with Metran specifications and serves as a tool for batch-level quality control.
Metran CoA mostly includes findings from lab analyses of a specific batch. For each Metran 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.
Metran may be tested according to a variety of international standards, such as European Pharmacopoeia (Metran EP), Metran JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Metran USP).
