DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 1M/s Dr Reddy's Laboratories Limited
02 1M/s Aarti Drugs ltd
03 1M/s CTX Lifesciences Pvt Ltd
04 1M/s Dasami lab Private Limited
05 1M/s Jubilant Pharmova Limited
06 1M/s. Lupin Manufacturing Solutions Limited
07 1M/s. Sun Pharmaceutical Industries Ltd
08 1M/sApitoria Pharma Private Limited
09 1M/sAssurgen Pharma Pvt ltd
10 1M/sMSN Life Sciences Pvt Ltd
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Date of Issue : 15-07-2025
Valid Till : 07-07-2028
Written Confirmation Number : WC-0067
Address of the Firm : Chemical Technical Operation’s Unit-VI,APIIC Industrial Estate, Pydibhimavaram...
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PharmaCompass offers a list of Eslicarbazepine Acetate 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 Eslicarbazepine Acetate manufacturer or Eslicarbazepine Acetate supplier for your needs.
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A Aptiom manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Aptiom, including repackagers and relabelers. The FDA regulates Aptiom manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Aptiom 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 Aptiom supplier is an individual or a company that provides Aptiom active pharmaceutical ingredient (API) or Aptiom finished formulations upon request. The Aptiom suppliers may include Aptiom API manufacturers, exporters, distributors and traders.
click here to find a list of Aptiom suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Aptiom written confirmation (Aptiom WC) is an official document issued by a regulatory agency to a Aptiom manufacturer, verifying that the manufacturing facility of a Aptiom active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Aptiom APIs or Aptiom finished pharmaceutical products to another nation, regulatory agencies frequently require a Aptiom WC (written confirmation) as part of the regulatory process.
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