Synopsis
Synopsis
0
USDMF
0
CEP/COS
0
JDMF
0
EU WC
0
KDMF
0
NDC API
0
VMF
0
FDF
0
FDA Orange Book
0
Europe
0
Canada
0
Australia
0
South Africa
DRUG PRODUCT COMPOSITIONS
0
EDQM
0
USP
0
JP
0
Others
0
US Patents
0
US Exclusivities
0
Health Canada Patents
0
Data Compilation #PharmaFlow
0
Stock Recap #PipelineProspector
0
Weekly News Recap #Phispers
0
News #PharmaBuzz
US Medicaid
NA
Annual Reports
NA
Finished Drug Prices
NA
1. 118443-89-3
2. Cefquinome Sulphate
3. Hr111v-sulfate
4. Cefquinome Sulfate [usan]
5. Hr111v-sulphate
6. (6r,7r)-7-[[(2z)-2-(2-amino-1,3-thiazol-4-yl)-2-methoxyiminoacetyl]amino]-8-oxo-3-(5,6,7,8-tetrahydroquinolin-1-ium-1-ylmethyl)-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate;sulfuric Acid
7. 3858k104dq
8. Unii-3858k104dq
9. 118443-88-2
10. 1-(((6r,7r)-7-((z)-2-(2-aminothiazol-4-yl)-2-(methoxyimino)acetamido)-2-carboxy-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-en-3-yl)methyl)-5,6,7,8-tetrahydroquinolin-1-ium Hydrogensulfate
11. Hr-111v-sulfate
12. Schembl988522
13. Cefquinome Sulfate [mi]
14. Chembl2103931
15. Cefquinome Sulfate [mart.]
16. Mfcd11864966
17. Akos025310170
18. Gs-3615
19. 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)-5,6,7,8-tetrahydroquinolinium Hydroxide, Inner Salt, 7(sup 2)-(z)-(o-methyloxime), Sulfate (1:1)
20. 1-{[(6r,7r)-7-[(2z)-2-(2-amino-1,3-thiazol-4-yl)-2-(methoxyimino)acetamido]-2-carboxy-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-en-3-yl]methyl}-5,6,7,8-tetrahydroquinolin-1-ium; Sulfuric Acid
21. Quinolinium, 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-(6.alpha.,7.beta.(z)))-, Sulfate (1:1)
22. Quinolinium, 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-(6.alpha.,7.beta.(z)))-, Sulphate (1:1)
23. Quinolinium, 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)))-, Sulfate (1:1)
Molecular Weight | 626.7 g/mol |
---|---|
Molecular Formula | C23H26N6O9S3 |
Hydrogen Bond Donor Count | 4 |
Hydrogen Bond Acceptor Count | 14 |
Rotatable Bond Count | 6 |
Exact Mass | 626.09233995 g/mol |
Monoisotopic Mass | 626.09233995 g/mol |
Topological Polar Surface Area | 290 Ų |
Heavy Atom Count | 41 |
Formal Charge | 0 |
Complexity | 1050 |
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 | 2 |
API Imports and Exports
Importing Country | Total Quantity (KGS) |
Average Price (USD/KGS) |
Number of Transactions |
---|
Upgrade, download data, analyse, strategize, subscribe with us
Regulatory Info :
Registration Country : South Korea
Brand Name : Cefnom
Dosage Form : Injectable
Dosage Strength : 25MG/ML
Packaging : 50ML, 100ML
Approval Date :
Application Number :
Regulatory Info :
Registration Country : South Korea
Regulatory Info :
Registration Country : China
Brand Name :
Dosage Form : Powder for Injection
Dosage Strength : 50MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : China
Regulatory Info :
Registration Country : China
Brand Name :
Dosage Form : Powder for Injection
Dosage Strength : 0.1G
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : China
Regulatory Info :
Registration Country : China
Brand Name :
Dosage Form : Powder for Injection
Dosage Strength : 0.2G
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : China
Regulatory Info :
Registration Country : China
Brand Name :
Dosage Form : Powder for Injection
Dosage Strength : 0.5G
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : China
Regulatory Info :
Registration Country : China
Brand Name :
Dosage Form : Sterilized Injection
Dosage Strength : 2.5%/50ML
Packaging : 50ml/100ml/250ml
Approval Date :
Application Number :
Regulatory Info :
Registration Country : China
Regulatory Info :
Registration Country : China
Brand Name :
Dosage Form : Sterilized Injection
Dosage Strength : 7.5%/100ML
Packaging : 50ml/100ml/250ml
Approval Date :
Application Number :
Regulatory Info :
Registration Country : China
Regulatory Info :
Registration Country : China
Brand Name :
Dosage Form : Intramammary Infusion
Dosage Strength : 75MG
Packaging : 8 g
Approval Date :
Application Number :
Regulatory Info :
Registration Country : China
Regulatory Info :
Registration Country : South Korea
Brand Name : Cefnom
Dosage Form : Injectable
Dosage Strength : 25MG/ML
Packaging : 50ML, 100ML
Approval Date :
Application Number :
Regulatory Info :
Registration Country : South Korea
Packaging : 50ML, 100ML
Regulatory Info :
Dosage : Injectable
Dosage Strength : 25MG/ML
Brand Name : Cefnom
Approval Date :
Application Number :
Registration Country : South Korea
Regulatory Info :
Registration Country : China
Brand Name :
Dosage Form : Powder for Injection
Dosage Strength : 50MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : China
Packaging :
Regulatory Info :
Dosage : Powder for Injection
Dosage Strength : 50MG
Brand Name :
Approval Date :
Application Number :
Registration Country : China
Regulatory Info :
Registration Country : China
Brand Name :
Dosage Form : Powder for Injection
Dosage Strength : 0.1G
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : China
Packaging :
Regulatory Info :
Dosage : Powder for Injection
Dosage Strength : 0.1G
Brand Name :
Approval Date :
Application Number :
Registration Country : China
Regulatory Info :
Registration Country : China
Brand Name :
Dosage Form : Powder for Injection
Dosage Strength : 0.2G
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : China
Packaging :
Regulatory Info :
Dosage : Powder for Injection
Dosage Strength : 0.2G
Brand Name :
Approval Date :
Application Number :
Registration Country : China
Regulatory Info :
Registration Country : China
Brand Name :
Dosage Form : Powder for Injection
Dosage Strength : 0.5G
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : China
Packaging :
Regulatory Info :
Dosage : Powder for Injection
Dosage Strength : 0.5G
Brand Name :
Approval Date :
Application Number :
Registration Country : China
Regulatory Info :
Registration Country : China
Brand Name :
Dosage Form : Sterilized Injection
Dosage Strength : 2.5%/50ML
Packaging : 50ml/100ml/250ml
Approval Date :
Application Number :
Regulatory Info :
Registration Country : China
Packaging : 50ml/100ml/250ml
Regulatory Info :
Dosage : Sterilized Injection
Dosage Strength : 2.5%/50ML
Brand Name :
Approval Date :
Application Number :
Registration Country : China
Regulatory Info :
Registration Country : China
Brand Name :
Dosage Form : Sterilized Injection
Dosage Strength : 7.5%/100ML
Packaging : 50ml/100ml/250ml
Approval Date :
Application Number :
Regulatory Info :
Registration Country : China
Packaging : 50ml/100ml/250ml
Regulatory Info :
Dosage : Sterilized Injection
Dosage Strength : 7.5%/100ML
Brand Name :
Approval Date :
Application Number :
Registration Country : China
Regulatory Info :
Registration Country : China
Brand Name :
Dosage Form : Intramammary Infusion
Dosage Strength : 75MG
Packaging : 8 g
Approval Date :
Application Number :
Regulatory Info :
Registration Country : China
Packaging : 8 g
Regulatory Info :
Dosage : Intramammary Infusion
Dosage Strength : 75MG
Brand Name :
Approval Date :
Application Number :
Registration Country : China
Market Place
ABOUT THIS PAGE
A Cefquinome Sulfate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cefquinome Sulfate, including repackagers and relabelers. The FDA regulates Cefquinome Sulfate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cefquinome Sulfate 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 Cefquinome Sulfate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cefquinome Sulfate supplier is an individual or a company that provides Cefquinome Sulfate active pharmaceutical ingredient (API) or Cefquinome Sulfate finished formulations upon request. The Cefquinome Sulfate suppliers may include Cefquinome Sulfate API manufacturers, exporters, distributors and traders.
click here to find a list of Cefquinome Sulfate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
Cefquinome Sulfate 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 Cefquinome Sulfate 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 Cefquinome Sulfate GMP manufacturer or Cefquinome Sulfate GMP API supplier for your needs.
A Cefquinome Sulfate CoA (Certificate of Analysis) is a formal document that attests to Cefquinome Sulfate's compliance with Cefquinome Sulfate specifications and serves as a tool for batch-level quality control.
Cefquinome Sulfate CoA mostly includes findings from lab analyses of a specific batch. For each Cefquinome Sulfate 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.
Cefquinome Sulfate may be tested according to a variety of international standards, such as European Pharmacopoeia (Cefquinome Sulfate EP), Cefquinome Sulfate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Cefquinome Sulfate USP).
LOOKING FOR A SUPPLIER?