01 1KOLON LIFE SCIENCE, INC.
02 1Laxai Life Sciences Private Limited
03 1SMS Pharmaceuticals Limited
04 1Tianish Laboratories Private Limited
01 1SUMATRIPTAN SUCCINATE
02 3Sumatriptan succinate
01 2India
02 1South Korea
03 1U.S.A
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. 564/A/22, Road No. 92, Jubilee Hills, Hyderabad-500096, Telangana, India
Initial Date of Registration : 2011-04-06
Latest Date of Registration : 2011-04-06
A Sumatriptan Succinate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sumatriptan Succinate, including repackagers and relabelers. The FDA regulates Sumatriptan Succinate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sumatriptan Succinate 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 Sumatriptan Succinate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sumatriptan Succinate supplier is an individual or a company that provides Sumatriptan Succinate active pharmaceutical ingredient (API) or Sumatriptan Succinate finished formulations upon request. The Sumatriptan Succinate suppliers may include Sumatriptan Succinate API manufacturers, exporters, distributors and traders.
click here to find a list of Sumatriptan Succinate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price 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 Sumatriptan Succinate Drug Master File in Japan (Sumatriptan Succinate JDMF) empowers Sumatriptan Succinate 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 Sumatriptan Succinate JDMF during the approval evaluation for pharmaceutical products. At the time of Sumatriptan Succinate 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 Sumatriptan Succinate suppliers with JDMF on PharmaCompass.
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