01 1MSN Laboratories Private Limited
01 1Pharmapia Co., Ltd.
01 1Gilteritinib fumarate
01 1India
Registrant Name : Pharmapia Co., Ltd.
Registration Date : 2025-03-31
Registration Number : 20250331-211-J-1804
Manufacturer Name : MSN Laboratories Private Lim...
Manufacturer Address : (Unit-ll) Sy. No. 50, 53, 53/A, 54 & 54/A, Kardanur (Village), Patancheru (Mandal), S...
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PharmaCompass offers a list of Gilteritinib Fumarate 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 Gilteritinib Fumarate manufacturer or Gilteritinib Fumarate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Gilteritinib Fumarate manufacturer or Gilteritinib Fumarate supplier.
PharmaCompass also assists you with knowing the Gilteritinib Fumarate API Price utilized in the formulation of products. Gilteritinib Fumarate API Price is not always fixed or binding as the Gilteritinib Fumarate Price is obtained through a variety of data sources. The Gilteritinib Fumarate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Gilteritinib Fumarate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Gilteritinib Fumarate, including repackagers and relabelers. The FDA regulates Gilteritinib Fumarate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Gilteritinib Fumarate 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 Gilteritinib Fumarate supplier is an individual or a company that provides Gilteritinib Fumarate active pharmaceutical ingredient (API) or Gilteritinib Fumarate finished formulations upon request. The Gilteritinib Fumarate suppliers may include Gilteritinib Fumarate API manufacturers, exporters, distributors and traders.
click here to find a list of Gilteritinib Fumarate 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 Gilteritinib Fumarate Drug Master File in Korea (Gilteritinib Fumarate KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Gilteritinib Fumarate. The MFDS reviews the Gilteritinib Fumarate KDMF as part of the drug registration process and uses the information provided in the Gilteritinib Fumarate KDMF to evaluate the safety and efficacy of the drug.
After submitting a Gilteritinib Fumarate 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 Gilteritinib Fumarate API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Gilteritinib Fumarate suppliers with KDMF on PharmaCompass.
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