01 1Hovione FarmaCiencia SA
01 1Daiichi Sankyo Korea Co., Ltd.
01 1Quizartinib HCl
01 1Portugal
Registrant Name : Daiichi Sankyo Korea Co., Ltd.
Registration Date : 2026-01-26
Registration Number : Su256-7-ND
Manufacturer Name : Hovione FarmaCiencia SA
Manufacturer Address : Sete Casas, 2674-506 Loures, Portugal
67
PharmaCompass offers a list of Quizartinib 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 Quizartinib manufacturer or Quizartinib supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Quizartinib manufacturer or Quizartinib supplier.
PharmaCompass also assists you with knowing the Quizartinib API Price utilized in the formulation of products. Quizartinib API Price is not always fixed or binding as the Quizartinib Price is obtained through a variety of data sources. The Quizartinib Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Quizartinib manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Quizartinib, including repackagers and relabelers. The FDA regulates Quizartinib manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Quizartinib API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Quizartinib supplier is an individual or a company that provides Quizartinib active pharmaceutical ingredient (API) or Quizartinib finished formulations upon request. The Quizartinib suppliers may include Quizartinib API manufacturers, exporters, distributors and traders.
click here to find a list of Quizartinib suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Quizartinib Drug Master File in Korea (Quizartinib KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Quizartinib. The MFDS reviews the Quizartinib KDMF as part of the drug registration process and uses the information provided in the Quizartinib KDMF to evaluate the safety and efficacy of the drug.
After submitting a Quizartinib KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their Quizartinib API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Quizartinib suppliers with KDMF on PharmaCompass.
