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
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A Boots Pharmacy Migraine Relief manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Boots Pharmacy Migraine Relief, including repackagers and relabelers. The FDA regulates Boots Pharmacy Migraine Relief manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Boots Pharmacy Migraine Relief 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 Boots Pharmacy Migraine Relief supplier is an individual or a company that provides Boots Pharmacy Migraine Relief active pharmaceutical ingredient (API) or Boots Pharmacy Migraine Relief finished formulations upon request. The Boots Pharmacy Migraine Relief suppliers may include Boots Pharmacy Migraine Relief API manufacturers, exporters, distributors and traders.
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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 Boots Pharmacy Migraine Relief Drug Master File in Japan (Boots Pharmacy Migraine Relief JDMF) empowers Boots Pharmacy Migraine Relief 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 Boots Pharmacy Migraine Relief JDMF during the approval evaluation for pharmaceutical products. At the time of Boots Pharmacy Migraine Relief JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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