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1. Sulacillin
1. 94935-63-4
2. Ampicillin Mixture With Sulbactam
3. Sulacillin
4. Ampicillin-sulbactam
5. (2s,5r,6r)-6-[[(2r)-2-amino-2-phenylacetyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic Acid;(1r,4s)-3,3-dimethyl-2,2,6-trioxo-2lambda6-thiabicyclo[3.2.0]heptane-4-carboxylic Acid
6. Sulbactam-ampicillin Mixt. (1:2)
7. Ampicillin-sulbactam Mixt.
8. Ampicillin And Sulbactam
9. Dtxsid60241694
10. 4-thia-1-azabicyclo(3.2.0)heptane-2-carboxylic Acid, 6-(((2r)-aminophenylacetyl)amino)-3,3-dimethyl-7-oxo-, (2s,5r,6r)-, Mixt. With (2s,5r)-3,3-dimethyl-7-oxo-thia-1-azabicyclo(3.2.0)heptane-2-carboxylic Acid 4,4-dioxide
11. 4-thia-1-azabicyclo(3.2.0)heptane-2-carboxylic Acid, 6-((aminophenylacetyl)amino)-3,3-dimethyl-7-oxo-, (2s-(2-alpha,5-alpha,6-beta(s*)))-, Mixt. With (2s-cis)-3,3-dimethyl-7-oxo-thia-1-azabicyclo(3.2.0)heptane-2-carboxylic Acid 4,4-dioxide
| Molecular Weight | 581.7 g/mol |
|---|---|
| Molecular Formula | C25H31N3O9S2 |
| Hydrogen Bond Donor Count | 4 |
| Hydrogen Bond Acceptor Count | 11 |
| Rotatable Bond Count | 5 |
| Exact Mass | 581.15017192 g/mol |
| Monoisotopic Mass | 581.15017192 g/mol |
| Topological Polar Surface Area | 235 Ų |
| Heavy Atom Count | 39 |
| Formal Charge | 0 |
| Complexity | 1000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 6 |
| Undefined Atom Stereocenter Count | 1 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 2 |
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ABOUT THIS PAGE
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PharmaCompass offers a list of Sulacillin API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Sulacillin manufacturer or Sulacillin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Sulacillin manufacturer or Sulacillin supplier.
A AMPICILLIN AND SULBACTAM STERILE MIXTURE manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of AMPICILLIN AND SULBACTAM STERILE MIXTURE, including repackagers and relabelers. The FDA regulates AMPICILLIN AND SULBACTAM STERILE MIXTURE manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. AMPICILLIN AND SULBACTAM STERILE MIXTURE 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 AMPICILLIN AND SULBACTAM STERILE MIXTURE manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A AMPICILLIN AND SULBACTAM STERILE MIXTURE supplier is an individual or a company that provides AMPICILLIN AND SULBACTAM STERILE MIXTURE active pharmaceutical ingredient (API) or AMPICILLIN AND SULBACTAM STERILE MIXTURE finished formulations upon request. The AMPICILLIN AND SULBACTAM STERILE MIXTURE suppliers may include AMPICILLIN AND SULBACTAM STERILE MIXTURE API manufacturers, exporters, distributors and traders.
click here to find a list of AMPICILLIN AND SULBACTAM STERILE MIXTURE suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A AMPICILLIN AND SULBACTAM STERILE MIXTURE DMF (Drug Master File) is a document detailing the whole manufacturing process of AMPICILLIN AND SULBACTAM STERILE MIXTURE active pharmaceutical ingredient (API) in detail. Different forms of AMPICILLIN AND SULBACTAM STERILE MIXTURE DMFs exist exist since differing nations have different regulations, such as AMPICILLIN AND SULBACTAM STERILE MIXTURE USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A AMPICILLIN AND SULBACTAM STERILE MIXTURE DMF submitted to regulatory agencies in the US is known as a USDMF. AMPICILLIN AND SULBACTAM STERILE MIXTURE USDMF includes data on AMPICILLIN AND SULBACTAM STERILE MIXTURE's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The AMPICILLIN AND SULBACTAM STERILE MIXTURE USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of AMPICILLIN AND SULBACTAM STERILE MIXTURE suppliers with USDMF on PharmaCompass.
A AMPICILLIN AND SULBACTAM STERILE MIXTURE written confirmation (AMPICILLIN AND SULBACTAM STERILE MIXTURE WC) is an official document issued by a regulatory agency to a AMPICILLIN AND SULBACTAM STERILE MIXTURE manufacturer, verifying that the manufacturing facility of a AMPICILLIN AND SULBACTAM STERILE MIXTURE active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting AMPICILLIN AND SULBACTAM STERILE MIXTURE APIs or AMPICILLIN AND SULBACTAM STERILE MIXTURE finished pharmaceutical products to another nation, regulatory agencies frequently require a AMPICILLIN AND SULBACTAM STERILE MIXTURE WC (written confirmation) as part of the regulatory process.
click here to find a list of AMPICILLIN AND SULBACTAM STERILE MIXTURE suppliers with Written Confirmation (WC) on PharmaCompass.
AMPICILLIN AND SULBACTAM STERILE MIXTURE 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 AMPICILLIN AND SULBACTAM STERILE MIXTURE GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right AMPICILLIN AND SULBACTAM STERILE MIXTURE GMP manufacturer or AMPICILLIN AND SULBACTAM STERILE MIXTURE GMP API supplier for your needs.
A AMPICILLIN AND SULBACTAM STERILE MIXTURE CoA (Certificate of Analysis) is a formal document that attests to AMPICILLIN AND SULBACTAM STERILE MIXTURE's compliance with AMPICILLIN AND SULBACTAM STERILE MIXTURE specifications and serves as a tool for batch-level quality control.
AMPICILLIN AND SULBACTAM STERILE MIXTURE CoA mostly includes findings from lab analyses of a specific batch. For each AMPICILLIN AND SULBACTAM STERILE MIXTURE 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.
AMPICILLIN AND SULBACTAM STERILE MIXTURE may be tested according to a variety of international standards, such as European Pharmacopoeia (AMPICILLIN AND SULBACTAM STERILE MIXTURE EP), AMPICILLIN AND SULBACTAM STERILE MIXTURE JP (Japanese Pharmacopeia) and the US Pharmacopoeia (AMPICILLIN AND SULBACTAM STERILE MIXTURE USP).