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1. Cefditoren
2. Cefditoren, Sodium Salt, (6r-(3(z),6alpha,7beta(z)))-isomer
3. Me 1206
4. Me-1206
1. Cefditoren Sodium
2. Cefditoren (sodium)
3. 104146-53-4
4. Sodium;(6r,7r)-7-[[(2z)-2-(2-amino-1,3-thiazol-4-yl)-2-methoxyiminoacetyl]amino]-3-[(z)-2-(4-methyl-1,3-thiazol-5-yl)ethenyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate
5. Cefditorensodium
6. C634tp4vz5
7. Me-1206
8. Hy-17452
9. Cs-0008424
10. 5-thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic Acid, 7-(((2z)-2-(2-amino-4-thiazolyl)-2-(methoxyimino)acetyl)amino)-3-((1z)-2-(4-methyl-5-thiazolyl)ethenyl)-8-oxo-, Sodium Salt (1:1), (6r,7r)-
| Molecular Weight | 528.6 g/mol |
|---|---|
| Molecular Formula | C19H17N6NaO5S3 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 12 |
| Rotatable Bond Count | 7 |
| Exact Mass | 528.03202547 g/mol |
| Monoisotopic Mass | 528.03202547 g/mol |
| Topological Polar Surface Area | 245 Ų |
| Heavy Atom Count | 34 |
| Formal Charge | 0 |
| Complexity | 934 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 2 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 2 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 2 |
Anti-Bacterial Agents
Substances that inhibit the growth or reproduction of BACTERIA. (See all compounds classified as Anti-Bacterial Agents.)
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ABOUT THIS PAGE
A Cefditoren Sodium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cefditoren Sodium, including repackagers and relabelers. The FDA regulates Cefditoren Sodium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cefditoren Sodium 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 Cefditoren Sodium supplier is an individual or a company that provides Cefditoren Sodium active pharmaceutical ingredient (API) or Cefditoren Sodium finished formulations upon request. The Cefditoren Sodium suppliers may include Cefditoren Sodium API manufacturers, exporters, distributors and traders.
Cefditoren Sodium 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 Cefditoren Sodium 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 Cefditoren Sodium GMP manufacturer or Cefditoren Sodium GMP API supplier for your needs.
A Cefditoren Sodium CoA (Certificate of Analysis) is a formal document that attests to Cefditoren Sodium's compliance with Cefditoren Sodium specifications and serves as a tool for batch-level quality control.
Cefditoren Sodium CoA mostly includes findings from lab analyses of a specific batch. For each Cefditoren Sodium 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.
Cefditoren Sodium may be tested according to a variety of international standards, such as European Pharmacopoeia (Cefditoren Sodium EP), Cefditoren Sodium JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Cefditoren Sodium USP).
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