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01 1M/s MSN Laboratories
02 1MSN Laboratories Pvt. Ltd.
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01 2Ruxolitinib Phosphate IH
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01 1WC-0349
02 1WC-0349A3
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01 2India
Date of Issue : 2022-09-02
Valid Till : 2025-05-05
Written Confirmation Number : WC-0349
Address of the Firm : MIs. MSN Laboratories Private Limited, Unit-II, sv. No, 50, Kardanur (Village), ...
Date of Issue : 2019-08-05
Valid Till : 2022-05-05
Written Confirmation Number : WC-0349A3
Address of the Firm : Unit-||, Sy. No. 50, Kardanur Village, Patti/Post Patancheru Mandal,Medak Distri...
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PharmaCompass offers a list of Ruxolitinib Phosphate 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 Ruxolitinib Phosphate manufacturer or Ruxolitinib Phosphate supplier for your needs.
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PharmaCompass also assists you with knowing the Ruxolitinib Phosphate API Price utilized in the formulation of products. Ruxolitinib Phosphate API Price is not always fixed or binding as the Ruxolitinib Phosphate Price is obtained through a variety of data sources. The Ruxolitinib Phosphate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Jakafi manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Jakafi, including repackagers and relabelers. The FDA regulates Jakafi manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Jakafi 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 Jakafi supplier is an individual or a company that provides Jakafi active pharmaceutical ingredient (API) or Jakafi finished formulations upon request. The Jakafi suppliers may include Jakafi API manufacturers, exporters, distributors and traders.
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A Jakafi written confirmation (Jakafi WC) is an official document issued by a regulatory agency to a Jakafi manufacturer, verifying that the manufacturing facility of a Jakafi active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Jakafi APIs or Jakafi finished pharmaceutical products to another nation, regulatory agencies frequently require a Jakafi WC (written confirmation) as part of the regulatory process.
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