01 1M/s Virchow Drugs Limited
02 1M/s. Virchow Drugs Limited
01 1Sulfasalazine(BP/USP)
02 1Sulphasalazine EP/BP
01 1WC-0235A1
02 1WC-235
01 2India
Date of Issue : 2019-11-07
Valid Till : 2022-07-02
Written Confirmation Number : WC-235
Address of the Firm : Sy. No. 639, Temple Road, Bonthapally(V), Jinnaram(M), Medak Dist, A.P
Date of Issue : 2020-05-12
Valid Till : 2022-07-02
Written Confirmation Number : WC-0235A1
Address of the Firm : Sy. No. 639, Temple Road, Bonthapally(V), Jinnaram(M), Medak Dist, A.P
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PharmaCompass offers a list of Sulfasalazine 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 Sulfasalazine manufacturer or Sulfasalazine supplier for your needs.
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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 EN-tabs manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Azulfidine EN-tabs, including repackagers and relabelers. The FDA regulates Azulfidine EN-tabs manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Azulfidine EN-tabs 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 EN-tabs supplier is an individual or a company that provides Azulfidine EN-tabs active pharmaceutical ingredient (API) or Azulfidine EN-tabs finished formulations upon request. The Azulfidine EN-tabs suppliers may include Azulfidine EN-tabs API manufacturers, exporters, distributors and traders.
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A Azulfidine EN-tabs written confirmation (Azulfidine EN-tabs WC) is an official document issued by a regulatory agency to a Azulfidine EN-tabs manufacturer, verifying that the manufacturing facility of a Azulfidine EN-tabs active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Azulfidine EN-tabs APIs or Azulfidine EN-tabs finished pharmaceutical products to another nation, regulatory agencies frequently require a Azulfidine EN-tabs WC (written confirmation) as part of the regulatory process.
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