01 1M/s IPCA Laboratories Ltd
02 1M/s Mangalam Drugs and Organics Ltd
01 1Furosemide BP/Ph.Eur./JP/USP
02 1Furosemide IH/BP/IP/USP/EP
01 1WC-0091
02 1WC-0473
01 2India
Date of Issue : 2025-06-19
Valid Till : 2028-07-02
Written Confirmation Number : WC-0091
Address of the Firm : P.O. Sejavta, District -Ratlam, (M.P.)-457001, India
Date of Issue : 2024-03-21
Valid Till : 2027-03-20
Written Confirmation Number : WC-0473
Address of the Firm : Unit-2, Plot No 1203, Ill Phase GIDC, Vapi -396195, Dist.-Valsad, Gujarat, India
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PharmaCompass offers a list of Furosemide 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 Furosemide manufacturer or Furosemide supplier for your needs.
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PharmaCompass also assists you with knowing the Furosemide API Price utilized in the formulation of products. Furosemide API Price is not always fixed or binding as the Furosemide Price is obtained through a variety of data sources. The Furosemide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Prefemin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Prefemin, including repackagers and relabelers. The FDA regulates Prefemin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Prefemin 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 Prefemin supplier is an individual or a company that provides Prefemin active pharmaceutical ingredient (API) or Prefemin finished formulations upon request. The Prefemin suppliers may include Prefemin API manufacturers, exporters, distributors and traders.
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A Prefemin written confirmation (Prefemin WC) is an official document issued by a regulatory agency to a Prefemin manufacturer, verifying that the manufacturing facility of a Prefemin active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Prefemin APIs or Prefemin finished pharmaceutical products to another nation, regulatory agencies frequently require a Prefemin WC (written confirmation) as part of the regulatory process.
click here to find a list of Prefemin suppliers with Written Confirmation (WC) on PharmaCompass.
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