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01 1M/s IPCA Laboratories Ltd
02 1M/s Mangalam Drugs and Organics Ltd
03 1M/s Unique Chemicals
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01 1Furosemide BP/EP
02 1Furosemide BP/Ph.Eur./USP/JP
03 1Furosemide IH/BP/IP/USP/EP
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01 1WC-0076
02 1WC-0091n
03 1WC-0473
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01 3India
Date of Issue : 2022-06-08
Valid Till : 2025-07-02
Written Confirmation Number : WC-0091n
Address of the Firm : P.O. Sejavta, Dist. Ratlam, Madhya Pradesh, India.
Date of Issue : 2022-06-07
Valid Till : 2025-07-02
Written Confirmation Number : WC-0076
Address of the Firm : Plot No.5, Phase-IV, G.I.D.C, Industrial Area, Panoli-394116, Dist-Bharuch, Guja...
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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A C12H11ClN2O5S manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of C12H11ClN2O5S, including repackagers and relabelers. The FDA regulates C12H11ClN2O5S manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. C12H11ClN2O5S 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 C12H11ClN2O5S supplier is an individual or a company that provides C12H11ClN2O5S active pharmaceutical ingredient (API) or C12H11ClN2O5S finished formulations upon request. The C12H11ClN2O5S suppliers may include C12H11ClN2O5S API manufacturers, exporters, distributors and traders.
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A C12H11ClN2O5S written confirmation (C12H11ClN2O5S WC) is an official document issued by a regulatory agency to a C12H11ClN2O5S manufacturer, verifying that the manufacturing facility of a C12H11ClN2O5S active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting C12H11ClN2O5S APIs or C12H11ClN2O5S finished pharmaceutical products to another nation, regulatory agencies frequently require a C12H11ClN2O5S WC (written confirmation) as part of the regulatory process.
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