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1. 148563-16-0
2. Schembl33281
3. Dtxsid10164006
4. Akos030504555
5. B1348
6. D04701
| Molecular Weight | 337.39 g/mol |
|---|---|
| Molecular Formula | C13H23NO7S |
| Hydrogen Bond Donor Count | 6 |
| Hydrogen Bond Acceptor Count | 8 |
| Rotatable Bond Count | 5 |
| Exact Mass | 337.11952325 g/mol |
| Monoisotopic Mass | 337.11952325 g/mol |
| Topological Polar Surface Area | 156 Ų |
| Heavy Atom Count | 22 |
| Formal Charge | 0 |
| Complexity | 309 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 1 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 2 |
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PharmaCompass offers a list of Levalbuterol Sulfate 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 Levalbuterol Sulfate manufacturer or Levalbuterol Sulfate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Levalbuterol Sulfate manufacturer or Levalbuterol Sulfate supplier.
PharmaCompass also assists you with knowing the Levalbuterol Sulfate API Price utilized in the formulation of products. Levalbuterol Sulfate API Price is not always fixed or binding as the Levalbuterol Sulfate Price is obtained through a variety of data sources. The Levalbuterol Sulfate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Levosalbutamol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Levosalbutamol, including repackagers and relabelers. The FDA regulates Levosalbutamol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Levosalbutamol 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 Levosalbutamol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Levosalbutamol supplier is an individual or a company that provides Levosalbutamol active pharmaceutical ingredient (API) or Levosalbutamol finished formulations upon request. The Levosalbutamol suppliers may include Levosalbutamol API manufacturers, exporters, distributors and traders.
click here to find a list of Levosalbutamol suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Levosalbutamol DMF (Drug Master File) is a document detailing the whole manufacturing process of Levosalbutamol active pharmaceutical ingredient (API) in detail. Different forms of Levosalbutamol DMFs exist exist since differing nations have different regulations, such as Levosalbutamol USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Levosalbutamol DMF submitted to regulatory agencies in the US is known as a USDMF. Levosalbutamol USDMF includes data on Levosalbutamol's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Levosalbutamol USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Levosalbutamol suppliers with USDMF on PharmaCompass.
A Levosalbutamol written confirmation (Levosalbutamol WC) is an official document issued by a regulatory agency to a Levosalbutamol manufacturer, verifying that the manufacturing facility of a Levosalbutamol active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Levosalbutamol APIs or Levosalbutamol finished pharmaceutical products to another nation, regulatory agencies frequently require a Levosalbutamol WC (written confirmation) as part of the regulatory process.
click here to find a list of Levosalbutamol suppliers with Written Confirmation (WC) on PharmaCompass.
Levosalbutamol 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 Levosalbutamol 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 Levosalbutamol GMP manufacturer or Levosalbutamol GMP API supplier for your needs.
A Levosalbutamol CoA (Certificate of Analysis) is a formal document that attests to Levosalbutamol's compliance with Levosalbutamol specifications and serves as a tool for batch-level quality control.
Levosalbutamol CoA mostly includes findings from lab analyses of a specific batch. For each Levosalbutamol 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.
Levosalbutamol may be tested according to a variety of international standards, such as European Pharmacopoeia (Levosalbutamol EP), Levosalbutamol JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Levosalbutamol USP).
