DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
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DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Date of Issue : 2025-05-28
Valid Till : 2028-06-25
Written Confirmation Number : WC-0035
Address of the Firm : Chemical Technical Operations, Unit -Ill, Plot No. 116,Sri Venkateswara Co-opera...
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PharmaCompass offers a list of Amlodipine Besylate 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 Amlodipine Besylate manufacturer or Amlodipine Besylate supplier for your needs.
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PharmaCompass also assists you with knowing the Amlodipine Besylate API Price utilized in the formulation of products. Amlodipine Besylate API Price is not always fixed or binding as the Amlodipine Besylate Price is obtained through a variety of data sources. The Amlodipine Besylate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A EXFORGE manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of EXFORGE, including repackagers and relabelers. The FDA regulates EXFORGE manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. EXFORGE 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 EXFORGE supplier is an individual or a company that provides EXFORGE active pharmaceutical ingredient (API) or EXFORGE finished formulations upon request. The EXFORGE suppliers may include EXFORGE API manufacturers, exporters, distributors and traders.
click here to find a list of EXFORGE suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A EXFORGE written confirmation (EXFORGE WC) is an official document issued by a regulatory agency to a EXFORGE manufacturer, verifying that the manufacturing facility of a EXFORGE active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting EXFORGE APIs or EXFORGE finished pharmaceutical products to another nation, regulatory agencies frequently require a EXFORGE WC (written confirmation) as part of the regulatory process.
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