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PharmaCompass offers a list of Foslevodopa 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 Foslevodopa manufacturer or Foslevodopa supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Foslevodopa manufacturer or Foslevodopa supplier.
PharmaCompass also assists you with knowing the Foslevodopa API Price utilized in the formulation of products. Foslevodopa API Price is not always fixed or binding as the Foslevodopa Price is obtained through a variety of data sources. The Foslevodopa Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Foslevodopa manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Foslevodopa, including repackagers and relabelers. The FDA regulates Foslevodopa manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Foslevodopa 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 Foslevodopa supplier is an individual or a company that provides Foslevodopa active pharmaceutical ingredient (API) or Foslevodopa finished formulations upon request. The Foslevodopa suppliers may include Foslevodopa API manufacturers, exporters, distributors and traders.
National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Foslevodopa as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Foslevodopa API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture Foslevodopa as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain Foslevodopa and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Foslevodopa NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Foslevodopa suppliers with NDC on PharmaCompass.
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