DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 1M/s Dr. Reddy's laboratories Ltd
02 1M/sDr. Reddy's Laboratories ltd
03 1M/s Apitoria Pharma Limited
01 2Fondaparinux Sodium IH
02 1Fondaparinux Sodium Ph. Eur
01 1WC-0017
02 1WC-0034Amended
03 1WC-0034n
01 3India
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Date of Issue : 2022-06-06
Valid Till : 2025-06-16
Written Confirmation Number : WC-0034Amended
Address of the Firm : Plot Nos. 1, 75A, 75B, 105, 110, 111 & 112, Sri Venkateswara Co-operative Indust...
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Date of Issue : 2022-06-06
Valid Till : 2025-06-16
Written Confirmation Number : WC-0034n
Address of the Firm : Plot Nos. 1, 75A, 75B, 105, 110, 111 & 112, Sri Venkateswara Co-operative Indust...
Date of Issue : 2022-06-06
Valid Till : 2025-06-10
Written Confirmation Number : WC-0017
Address of the Firm : Unit-II, SurveyNo.:10&13,Gaddapotharam (Village), IDA-Kazipally, Jinnaram (Manda...
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PharmaCompass offers a list of Fondaparinux Sodium 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 Fondaparinux Sodium manufacturer or Fondaparinux Sodium supplier for your needs.
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PharmaCompass also assists you with knowing the Fondaparinux Sodium API Price utilized in the formulation of products. Fondaparinux Sodium API Price is not always fixed or binding as the Fondaparinux Sodium Price is obtained through a variety of data sources. The Fondaparinux Sodium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Arixtra manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Arixtra, including repackagers and relabelers. The FDA regulates Arixtra manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Arixtra 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 Arixtra supplier is an individual or a company that provides Arixtra active pharmaceutical ingredient (API) or Arixtra finished formulations upon request. The Arixtra suppliers may include Arixtra API manufacturers, exporters, distributors and traders.
click here to find a list of Arixtra suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Arixtra written confirmation (Arixtra WC) is an official document issued by a regulatory agency to a Arixtra manufacturer, verifying that the manufacturing facility of a Arixtra active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Arixtra APIs or Arixtra finished pharmaceutical products to another nation, regulatory agencies frequently require a Arixtra WC (written confirmation) as part of the regulatory process.
click here to find a list of Arixtra suppliers with Written Confirmation (WC) on PharmaCompass.
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