01 1M/s Eskay Iodine Pvt ltd
01 1Di-Iodohydroxyquinoline (Iodoquninol) USP
01 1WC-0298
01 1India
Di-Iodohydroxyquinoline (Iodoquninol) USP
Date of Issue : 2023-12-07
Valid Till : 2026-11-06
Written Confirmation Number : WC-0298
Address of the Firm : Plot No.907/2, Jhagadia GIDC Estate, Jhagadia Dist-Bharuch-393 110, Gujarat, Ind...
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PharmaCompass offers a list of Iodoquinol 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 Iodoquinol manufacturer or Iodoquinol supplier for your needs.
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PharmaCompass also assists you with knowing the Iodoquinol API Price utilized in the formulation of products. Iodoquinol API Price is not always fixed or binding as the Iodoquinol Price is obtained through a variety of data sources. The Iodoquinol Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Fluoraquin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fluoraquin, including repackagers and relabelers. The FDA regulates Fluoraquin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fluoraquin 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 Fluoraquin supplier is an individual or a company that provides Fluoraquin active pharmaceutical ingredient (API) or Fluoraquin finished formulations upon request. The Fluoraquin suppliers may include Fluoraquin API manufacturers, exporters, distributors and traders.
click here to find a list of Fluoraquin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Fluoraquin written confirmation (Fluoraquin WC) is an official document issued by a regulatory agency to a Fluoraquin manufacturer, verifying that the manufacturing facility of a Fluoraquin active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Fluoraquin APIs or Fluoraquin finished pharmaceutical products to another nation, regulatory agencies frequently require a Fluoraquin WC (written confirmation) as part of the regulatory process.
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