DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

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01 1M/s Dr Reddys laboratories Limited
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01 1Lumateperone Tosylate IH
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01 1WC-0390
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01 1India
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Date of Issue : 2022-07-28
Valid Till : 2025-11-30
Written Confirmation Number : WC-0390
Address of the Firm : Devunipalavalasa Village, Ranasthalam Mandal, Srikakulam District -532409, Andhr...
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PharmaCompass offers a list of Lumateperone Tosylate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Lumateperone Tosylate manufacturer or Lumateperone Tosylate supplier for your needs.
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A Lumateperone manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lumateperone, including repackagers and relabelers. The FDA regulates Lumateperone manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lumateperone API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Lumateperone manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Lumateperone supplier is an individual or a company that provides Lumateperone active pharmaceutical ingredient (API) or Lumateperone finished formulations upon request. The Lumateperone suppliers may include Lumateperone API manufacturers, exporters, distributors and traders.
click here to find a list of Lumateperone suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Lumateperone written confirmation (Lumateperone WC) is an official document issued by a regulatory agency to a Lumateperone manufacturer, verifying that the manufacturing facility of a Lumateperone active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Lumateperone APIs or Lumateperone finished pharmaceutical products to another nation, regulatory agencies frequently require a Lumateperone WC (written confirmation) as part of the regulatory process.
click here to find a list of Lumateperone suppliers with Written Confirmation (WC) on PharmaCompass.
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