Shandong Loncom is an R&D-focused manufacturer of Anti-cancer APIs.
01 1Shandong Loncom Pharmaceutical Co. Ltd.
01 1Dotinurad
01 1SD250073
01 1China
Shandong Loncom is an R&D-focused manufacturer of Anti-cancer APIs.
Date of Issue : 2025-07-17
Valid Till : 2028-08-26
Written Confirmation Number : SD250073
Address of the Firm : No. 127, Qizhong Avenue, Qihe County, Dezhou City, Shandong Province, China
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PharmaCompass offers a list of Dotinurad 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 Dotinurad manufacturer or Dotinurad supplier for your needs.
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PharmaCompass also assists you with knowing the Dotinurad API Price utilized in the formulation of products. Dotinurad API Price is not always fixed or binding as the Dotinurad Price is obtained through a variety of data sources. The Dotinurad Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Dotinurad manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dotinurad, including repackagers and relabelers. The FDA regulates Dotinurad manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dotinurad 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 Dotinurad supplier is an individual or a company that provides Dotinurad active pharmaceutical ingredient (API) or Dotinurad finished formulations upon request. The Dotinurad suppliers may include Dotinurad API manufacturers, exporters, distributors and traders.
click here to find a list of Dotinurad suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Dotinurad written confirmation (Dotinurad WC) is an official document issued by a regulatory agency to a Dotinurad manufacturer, verifying that the manufacturing facility of a Dotinurad active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Dotinurad APIs or Dotinurad finished pharmaceutical products to another nation, regulatory agencies frequently require a Dotinurad WC (written confirmation) as part of the regulatory process.
click here to find a list of Dotinurad suppliers with Written Confirmation (WC) on PharmaCompass.
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