DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 1M/s Dr.Reddys Laboratories Limited
02 1M/sFresenius Kabi Oncology Ltd
03 1M/sMSN laboratories Pvt Lt
04 1M/sSionc Pharmaceuticals Pvt ltd
01 4Carfilzomib IH
01 1WC-0039
02 1WC-0115
03 1WC-0273
04 1WC-0349
01 4India
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Date of Issue : 2025-06-20
Valid Till : 2028-07-07
Written Confirmation Number : WC-0039
Address of the Firm : UNIT-I, Plot Nos. 137, 138, 145 & 146, Sri Venkateswara Co-operative Industrial ...
Date of Issue : 2025-11-12
Valid Till : 2028-11-11
Written Confirmation Number : WC-0115
Address of the Firm : D-35, Industrial Area, Kalyani, Dist-Nadia-741235, West Bengal
Date of Issue : 2025-09-19
Valid Till : 2028-05-05
Written Confirmation Number : WC-0349
Address of the Firm : Unit-II, Sy. Nos. 50, 53, 53/A, 54 & 54/A,Kardanur (Village), Patancheru (Mandal...
Date of Issue : 2023-11-15
Valid Till : 2026-05-11
Written Confirmation Number : WC-0273
Address of the Firm : Plot No: 34A, Road No: 1, Jawaharlal Nehru Pharma City, Thanam Village, Parawada...
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A AB01565867_02 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of AB01565867_02, including repackagers and relabelers. The FDA regulates AB01565867_02 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. AB01565867_02 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 AB01565867_02 supplier is an individual or a company that provides AB01565867_02 active pharmaceutical ingredient (API) or AB01565867_02 finished formulations upon request. The AB01565867_02 suppliers may include AB01565867_02 API manufacturers, exporters, distributors and traders.
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A AB01565867_02 written confirmation (AB01565867_02 WC) is an official document issued by a regulatory agency to a AB01565867_02 manufacturer, verifying that the manufacturing facility of a AB01565867_02 active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting AB01565867_02 APIs or AB01565867_02 finished pharmaceutical products to another nation, regulatory agencies frequently require a AB01565867_02 WC (written confirmation) as part of the regulatory process.
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