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 Diiodohidroxiquinoleina manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Diiodohidroxiquinoleina, including repackagers and relabelers. The FDA regulates Diiodohidroxiquinoleina manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Diiodohidroxiquinoleina 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 Diiodohidroxiquinoleina supplier is an individual or a company that provides Diiodohidroxiquinoleina active pharmaceutical ingredient (API) or Diiodohidroxiquinoleina finished formulations upon request. The Diiodohidroxiquinoleina suppliers may include Diiodohidroxiquinoleina API manufacturers, exporters, distributors and traders.
click here to find a list of Diiodohidroxiquinoleina suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Diiodohidroxiquinoleina written confirmation (Diiodohidroxiquinoleina WC) is an official document issued by a regulatory agency to a Diiodohidroxiquinoleina manufacturer, verifying that the manufacturing facility of a Diiodohidroxiquinoleina active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Diiodohidroxiquinoleina APIs or Diiodohidroxiquinoleina finished pharmaceutical products to another nation, regulatory agencies frequently require a Diiodohidroxiquinoleina WC (written confirmation) as part of the regulatory process.
click here to find a list of Diiodohidroxiquinoleina suppliers with Written Confirmation (WC) on PharmaCompass.
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