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01 Sterling Pharma Solutions Limited (1)
01 Pexidartinib HCl (1)
01 United Kingdom (1)
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PharmaCompass offers a list of Pexidartinib hydrochloride 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 Pexidartinib hydrochloride manufacturer or Pexidartinib hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Pexidartinib hydrochloride manufacturer or Pexidartinib hydrochloride supplier.
PharmaCompass also assists you with knowing the Pexidartinib hydrochloride API Price utilized in the formulation of products. Pexidartinib hydrochloride API Price is not always fixed or binding as the Pexidartinib hydrochloride Price is obtained through a variety of data sources. The Pexidartinib hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Pexidartinib hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Pexidartinib hydrochloride, including repackagers and relabelers. The FDA regulates Pexidartinib hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Pexidartinib hydrochloride 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 Pexidartinib hydrochloride supplier is an individual or a company that provides Pexidartinib hydrochloride active pharmaceutical ingredient (API) or Pexidartinib hydrochloride finished formulations upon request. The Pexidartinib hydrochloride suppliers may include Pexidartinib hydrochloride 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 Pexidartinib hydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Pexidartinib hydrochloride 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 Pexidartinib hydrochloride 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 Pexidartinib hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Pexidartinib hydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Pexidartinib hydrochloride suppliers with NDC on PharmaCompass.
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