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01 1Hetero Drugs
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01 1FOSTAMATINIB DISODIUM HEXAHYDRATE
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01 1India
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01 1Active
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01 1Complete
GDUFA
DMF Review : Complete
Rev. Date : 2022-03-04
Pay. Date : 2022-01-05
DMF Number : 36629
Submission : 2022-02-04
Status : Active
Type : II
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PharmaCompass offers a list of Fostamatinib Disodium Hexahydrate 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 Fostamatinib Disodium Hexahydrate manufacturer or Fostamatinib Disodium Hexahydrate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Fostamatinib Disodium Hexahydrate manufacturer or Fostamatinib Disodium Hexahydrate supplier.
PharmaCompass also assists you with knowing the Fostamatinib Disodium Hexahydrate API Price utilized in the formulation of products. Fostamatinib Disodium Hexahydrate API Price is not always fixed or binding as the Fostamatinib Disodium Hexahydrate Price is obtained through a variety of data sources. The Fostamatinib Disodium Hexahydrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Fostamatinib manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fostamatinib, including repackagers and relabelers. The FDA regulates Fostamatinib manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fostamatinib 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 Fostamatinib supplier is an individual or a company that provides Fostamatinib active pharmaceutical ingredient (API) or Fostamatinib finished formulations upon request. The Fostamatinib suppliers may include Fostamatinib API manufacturers, exporters, distributors and traders.
click here to find a list of Fostamatinib suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Fostamatinib DMF (Drug Master File) is a document detailing the whole manufacturing process of Fostamatinib active pharmaceutical ingredient (API) in detail. Different forms of Fostamatinib DMFs exist exist since differing nations have different regulations, such as Fostamatinib USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Fostamatinib DMF submitted to regulatory agencies in the US is known as a USDMF. Fostamatinib USDMF includes data on Fostamatinib's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Fostamatinib USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Fostamatinib suppliers with USDMF on PharmaCompass.
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