01 1M/sValens Molecules Private Limited
01 1Sulfasalazine USP/BP/Ph. Eur
01 1WC-0261n
01 1India
Date of Issue : 2021-05-28
Valid Till : 2023-03-22
Written Confirmation Number : WC-0261n
Address of the Firm : Plot No. 11, Road No. 2, Industrial Estate, Medchal-Malkajgiri - 501 401, Telang...
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PharmaCompass also assists you with knowing the Sulfasalazine API Price utilized in the formulation of products. Sulfasalazine API Price is not always fixed or binding as the Sulfasalazine Price is obtained through a variety of data sources. The Sulfasalazine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Azulfidine;Salazopyrin;Sulphasalazine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Azulfidine;Salazopyrin;Sulphasalazine, including repackagers and relabelers. The FDA regulates Azulfidine;Salazopyrin;Sulphasalazine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Azulfidine;Salazopyrin;Sulphasalazine 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 Azulfidine;Salazopyrin;Sulphasalazine supplier is an individual or a company that provides Azulfidine;Salazopyrin;Sulphasalazine active pharmaceutical ingredient (API) or Azulfidine;Salazopyrin;Sulphasalazine finished formulations upon request. The Azulfidine;Salazopyrin;Sulphasalazine suppliers may include Azulfidine;Salazopyrin;Sulphasalazine API manufacturers, exporters, distributors and traders.
click here to find a list of Azulfidine;Salazopyrin;Sulphasalazine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Azulfidine;Salazopyrin;Sulphasalazine written confirmation (Azulfidine;Salazopyrin;Sulphasalazine WC) is an official document issued by a regulatory agency to a Azulfidine;Salazopyrin;Sulphasalazine manufacturer, verifying that the manufacturing facility of a Azulfidine;Salazopyrin;Sulphasalazine active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Azulfidine;Salazopyrin;Sulphasalazine APIs or Azulfidine;Salazopyrin;Sulphasalazine finished pharmaceutical products to another nation, regulatory agencies frequently require a Azulfidine;Salazopyrin;Sulphasalazine WC (written confirmation) as part of the regulatory process.
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