01 1M/s Emcure Pharmaceuticals Limited
01 1Cidofovir USP
01 1WC-0226
01 1India
Date of Issue : 2025-09-26
Valid Till : 2028-07-02
Written Confirmation Number : WC-0226
Address of the Firm : D-24 & D-24/1, M.I.D.C., Kurkumbh, Taluka: Daund, District. Pune -413802, Mahara...
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PharmaCompass offers a list of Cidofovir 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 Cidofovir manufacturer or Cidofovir supplier for your needs.
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PharmaCompass also assists you with knowing the Cidofovir API Price utilized in the formulation of products. Cidofovir API Price is not always fixed or binding as the Cidofovir Price is obtained through a variety of data sources. The Cidofovir Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A cidofovir, sodium salt manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of cidofovir, sodium salt, including repackagers and relabelers. The FDA regulates cidofovir, sodium salt manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. cidofovir, sodium salt 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 cidofovir, sodium salt supplier is an individual or a company that provides cidofovir, sodium salt active pharmaceutical ingredient (API) or cidofovir, sodium salt finished formulations upon request. The cidofovir, sodium salt suppliers may include cidofovir, sodium salt API manufacturers, exporters, distributors and traders.
click here to find a list of cidofovir, sodium salt suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A cidofovir, sodium salt written confirmation (cidofovir, sodium salt WC) is an official document issued by a regulatory agency to a cidofovir, sodium salt manufacturer, verifying that the manufacturing facility of a cidofovir, sodium salt active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting cidofovir, sodium salt APIs or cidofovir, sodium salt finished pharmaceutical products to another nation, regulatory agencies frequently require a cidofovir, sodium salt WC (written confirmation) as part of the regulatory process.
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