DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 1Dr. Reddy's Laboratories Ltd.
02 1KOLON LIFE SCIENCE, INC.
03 1Laxai Life Sciences Private Limited
04 1Matrix Pharmacorp Private Limited
05 1SMS Pharmaceuticals Limited
01 1SUMATRIPTAN SUCCINATE
02 1Sumatriptan Succinate “CTO5”
03 3Sumatriptan succinate
01 3India
02 1South Korea
03 1U.S.A
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Registration Number : 308MF10006
Registrant's Address : 8-2-337, Road No. 3,Banjara Hills,Hyderabad 500 034,TELANGANA,INDIA
Initial Date of Registration : 2026-01-08
Latest Date of Registration : 2026-01-08
Registration Number : 223MF10060
Registrant's Address : 110, MAGOKDONG-RO, GANGSEO-GU, SEOUL, KOREA
Initial Date of Registration : 2011-04-28
Latest Date of Registration : 2012-05-21
Registration Number : 228MF10195
Registrant's Address : Plot No. 72, H. No.8-2-334/3&4 Road No. 5, Opp. SBI Executive Enclave, Banjara Hills,...
Initial Date of Registration : 2016-10-11
Latest Date of Registration : 2017-04-11
Registration Number : 221MF10241
Registrant's Address : 3rd Floor, Venturest Plaza, Plot No. 40 & 41, Road Number 2, Financial District, Nana...
Initial Date of Registration : 2009-11-16
Latest Date of Registration : 2009-11-16
Registration Number : 223MF10048
Registrant's Address : Plot No. 14, 99 and 100, IDA, Pashamylaram Phase-II, Patancheru, Sangareddy District ...
Initial Date of Registration : 2011-04-06
Latest Date of Registration : 2011-04-06
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A Illument manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Illument, including repackagers and relabelers. The FDA regulates Illument manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Illument 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 Illument manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Illument supplier is an individual or a company that provides Illument active pharmaceutical ingredient (API) or Illument finished formulations upon request. The Illument suppliers may include Illument API manufacturers, exporters, distributors and traders.
click here to find a list of Illument suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Illument Drug Master File in Japan (Illument JDMF) empowers Illument API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Illument JDMF during the approval evaluation for pharmaceutical products. At the time of Illument JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Illument suppliers with JDMF on PharmaCompass.
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