DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 2M/s Dr Reddy's Laboratories Limited
02 1M/s Aurore Pharmaceuticals Private limited
03 1M/s Centaur Pharmaceuticals Pvt Ltd
04 1M/s Chromo laboratories India Pvt ltd
05 1M/s Glenmark Life Sciences Limited
06 1M/s IPCA Laboratories Ltd
07 1M/s Lupin Ltd
08 1M/s Symed Labs Limited
09 1M/sMacleods pharmaceuticals Limited
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Date of Issue : 2022-06-07
Valid Till : 2025-07-07
Written Confirmation Number : WC-0067
Address of the Firm : Chemical Technical Operations Unit-VI, APIIC Industrial Estate, Pydibhimavaram V...
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Date of Issue : 2022-06-07
Valid Till : 2025-07-07
Written Confirmation Number : WC-0067
Address of the Firm : Chemical Technical Operations Unit-VI, APIIC Industrial Estate, Pydibhimavaram V...
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PharmaCompass offers a list of Eszopiclone 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 Eszopiclone manufacturer or Eszopiclone supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Eszopiclone manufacturer or Eszopiclone supplier.
PharmaCompass also assists you with knowing the Eszopiclone API Price utilized in the formulation of products. Eszopiclone API Price is not always fixed or binding as the Eszopiclone Price is obtained through a variety of data sources. The Eszopiclone Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Lunivia manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lunivia, including repackagers and relabelers. The FDA regulates Lunivia manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lunivia 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 Lunivia manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Lunivia supplier is an individual or a company that provides Lunivia active pharmaceutical ingredient (API) or Lunivia finished formulations upon request. The Lunivia suppliers may include Lunivia API manufacturers, exporters, distributors and traders.
click here to find a list of Lunivia suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Lunivia written confirmation (Lunivia WC) is an official document issued by a regulatory agency to a Lunivia manufacturer, verifying that the manufacturing facility of a Lunivia active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Lunivia APIs or Lunivia finished pharmaceutical products to another nation, regulatory agencies frequently require a Lunivia WC (written confirmation) as part of the regulatory process.
click here to find a list of Lunivia suppliers with Written Confirmation (WC) on PharmaCompass.
We have 9 companies offering Lunivia
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