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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PharmaCompass offers a list of Sumatriptan 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 Sumatriptan manufacturer or Sumatriptan supplier for your needs.
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PharmaCompass also assists you with knowing the Sumatriptan API Price utilized in the formulation of products. Sumatriptan API Price is not always fixed or binding as the Sumatriptan Price is obtained through a variety of data sources. The Sumatriptan Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A C14H21N3O2S manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of C14H21N3O2S, including repackagers and relabelers. The FDA regulates C14H21N3O2S manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. C14H21N3O2S 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 C14H21N3O2S supplier is an individual or a company that provides C14H21N3O2S active pharmaceutical ingredient (API) or C14H21N3O2S finished formulations upon request. The C14H21N3O2S suppliers may include C14H21N3O2S API manufacturers, exporters, distributors and traders.
click here to find a list of C14H21N3O2S 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 C14H21N3O2S Drug Master File in Japan (C14H21N3O2S JDMF) empowers C14H21N3O2S 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 C14H21N3O2S JDMF during the approval evaluation for pharmaceutical products. At the time of C14H21N3O2S 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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