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01 1Yamasa Corporation
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01 1DIQUAFOSOL TETRASODIUM
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01 1Japan
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01 1Inactive
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01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 14100
Submission : 1999-04-28
Status : Inactive
Type : II
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PharmaCompass offers a list of Diquafosol 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 Diquafosol manufacturer or Diquafosol supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Diquafosol manufacturer or Diquafosol supplier.
PharmaCompass also assists you with knowing the Diquafosol API Price utilized in the formulation of products. Diquafosol API Price is not always fixed or binding as the Diquafosol Price is obtained through a variety of data sources. The Diquafosol Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Diquas manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Diquas, including repackagers and relabelers. The FDA regulates Diquas manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Diquas API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Diquas manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Diquas supplier is an individual or a company that provides Diquas active pharmaceutical ingredient (API) or Diquas finished formulations upon request. The Diquas suppliers may include Diquas API manufacturers, exporters, distributors and traders.
click here to find a list of Diquas suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Diquas DMF (Drug Master File) is a document detailing the whole manufacturing process of Diquas active pharmaceutical ingredient (API) in detail. Different forms of Diquas DMFs exist exist since differing nations have different regulations, such as Diquas USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Diquas DMF submitted to regulatory agencies in the US is known as a USDMF. Diquas USDMF includes data on Diquas's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Diquas USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Diquas suppliers with USDMF on PharmaCompass.
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