01 1HARMAN FINOCHEM LIMITED
01 1Fospropofol Disodium
01 1India
NDC Package Code : 66064-1034
Start Marketing Date : 2020-02-01
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (5kg/5kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Fospropofol 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 Fospropofol manufacturer or Fospropofol supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Fospropofol manufacturer or Fospropofol supplier.
PharmaCompass also assists you with knowing the Fospropofol API Price utilized in the formulation of products. Fospropofol API Price is not always fixed or binding as the Fospropofol Price is obtained through a variety of data sources. The Fospropofol Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Fospropofol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fospropofol, including repackagers and relabelers. The FDA regulates Fospropofol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fospropofol 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 Fospropofol supplier is an individual or a company that provides Fospropofol active pharmaceutical ingredient (API) or Fospropofol finished formulations upon request. The Fospropofol suppliers may include Fospropofol API manufacturers, exporters, distributors and traders.
click here to find a list of Fospropofol suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
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 Fospropofol as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Fospropofol 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 Fospropofol 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 Fospropofol and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Fospropofol NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Fospropofol suppliers with NDC on PharmaCompass.
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