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1. Meropenem - Vaborbactam
2. Meropenem And Vaborbactam
3. Meropenem Vaborbactam Drug Combination
4. Vabomere
1. Meropenem & Vaborbactam
2. Meropenem + Vaborbactam
3. 2031124-72-6
4. Vabomere
5. Meropenem / Vaborbactam
6. Meropenem And Vaborbactam
7. Meropenem Mixture With Vaborbactam
8. (4r,5s,6s)-3-[(3s,5s)-5-(dimethylcarbamoyl)pyrrolidin-3-yl]sulfanyl-6-[(1r)-1-hydroxyethyl]-4-methyl-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylic Acid;2-[(3r,6s)-2-hydroxy-3-[(2-thiophen-2-ylacetyl)amino]oxaborinan-6-yl]acetic Acid
| Molecular Weight | 680.6 g/mol |
|---|---|
| Molecular Formula | C29H41BN4O10S2 |
| Hydrogen Bond Donor Count | 6 |
| Hydrogen Bond Acceptor Count | 13 |
| Rotatable Bond Count | 10 |
| Exact Mass | 680.2357160 g/mol |
| Monoisotopic Mass | 680.2357160 g/mol |
| Topological Polar Surface Area | 260 Ų |
| Heavy Atom Count | 46 |
| Formal Charge | 0 |
| Complexity | 1050 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 8 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 2 |
J - Antiinfectives for systemic use
J01 - Antibacterials for systemic use
J01D - Other beta-lactam antibacterials
J01DH - Carbapenems
J01DH52 - Meropenem and vaborbactam
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PharmaCompass offers a list of Meropenem And Vaborbactam 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 Meropenem And Vaborbactam manufacturer or Meropenem And Vaborbactam supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Meropenem And Vaborbactam manufacturer or Meropenem And Vaborbactam supplier.
PharmaCompass also assists you with knowing the Meropenem And Vaborbactam API Price utilized in the formulation of products. Meropenem And Vaborbactam API Price is not always fixed or binding as the Meropenem And Vaborbactam Price is obtained through a variety of data sources. The Meropenem And Vaborbactam Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Vabomere manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Vabomere, including repackagers and relabelers. The FDA regulates Vabomere manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Vabomere 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 Vabomere supplier is an individual or a company that provides Vabomere active pharmaceutical ingredient (API) or Vabomere finished formulations upon request. The Vabomere suppliers may include Vabomere API manufacturers, exporters, distributors and traders.
Vabomere 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 Vabomere 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 Vabomere GMP manufacturer or Vabomere GMP API supplier for your needs.
A Vabomere CoA (Certificate of Analysis) is a formal document that attests to Vabomere's compliance with Vabomere specifications and serves as a tool for batch-level quality control.
Vabomere CoA mostly includes findings from lab analyses of a specific batch. For each Vabomere 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.
Vabomere may be tested according to a variety of international standards, such as European Pharmacopoeia (Vabomere EP), Vabomere JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Vabomere USP).
