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PharmaCompass offers a list of Deutivacaftor 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 Deutivacaftor manufacturer or Deutivacaftor supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Deutivacaftor manufacturer or Deutivacaftor supplier.
PharmaCompass also assists you with knowing the Deutivacaftor API Price utilized in the formulation of products. Deutivacaftor API Price is not always fixed or binding as the Deutivacaftor Price is obtained through a variety of data sources. The Deutivacaftor Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Deutivacaftor manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Deutivacaftor, including repackagers and relabelers. The FDA regulates Deutivacaftor manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Deutivacaftor 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 Deutivacaftor supplier is an individual or a company that provides Deutivacaftor active pharmaceutical ingredient (API) or Deutivacaftor finished formulations upon request. The Deutivacaftor suppliers may include Deutivacaftor 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 Deutivacaftor as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Deutivacaftor 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 Deutivacaftor 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 Deutivacaftor and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Deutivacaftor NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Deutivacaftor suppliers with NDC on PharmaCompass.
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