01 1Alives Life Sciences Limited
02 2ILDONG PHARMACEUTICAL CO. , LTD.
03 1ScinoPharm Taiwan, Ltd.
04 1Siegfried Ltd
01 5Topiramate
01 1India
02 2South Korea
03 1Switzerland
04 1Taiwan
Registration Number : 227MF10208
Registrant's Address : 4th Floor, OIA House, 470, Cardinal Gracious Road, Andheri East Mumbai 400099, Mahara...
Initial Date of Registration : 2015-08-11
Latest Date of Registration : 2016-12-14
Registration Number : 301MF10026
Registrant's Address : 2, Baumoe-ro 27-gil, Seocho-gu, Seoul, Korea
Initial Date of Registration : 2019-07-04
Latest Date of Registration : 2019-07-04
Registration Number : 227MF10206
Registrant's Address : 2, Baumoe-ro 27-gil, Seocho-gu, Seoul, Korea
Initial Date of Registration : 2015-08-10
Latest Date of Registration : 2016-09-08
Registration Number : 301MF10073
Registrant's Address : No. 1, Nan-Ke 8th Road, Shan-Hua, Tainan 741014, Taiwan
Initial Date of Registration : 2019-10-08
Latest Date of Registration : 2023-09-06
Registration Number : 229MF10116
Registrant's Address : Untere Bru(¨)hlstrasse 4, CH-4800 Zofingen Switzerland
Initial Date of Registration : 2017-07-05
Latest Date of Registration : 2017-07-05
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PharmaCompass offers a list of Topiramate 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 Topiramate manufacturer or Topiramate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Topiramate manufacturer or Topiramate supplier.
PharmaCompass also assists you with knowing the Topiramate API Price utilized in the formulation of products. Topiramate API Price is not always fixed or binding as the Topiramate Price is obtained through a variety of data sources. The Topiramate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Trokendi XR manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Trokendi XR, including repackagers and relabelers. The FDA regulates Trokendi XR manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Trokendi XR 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 Trokendi XR manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Trokendi XR supplier is an individual or a company that provides Trokendi XR active pharmaceutical ingredient (API) or Trokendi XR finished formulations upon request. The Trokendi XR suppliers may include Trokendi XR API manufacturers, exporters, distributors and traders.
click here to find a list of Trokendi XR 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 Trokendi XR Drug Master File in Japan (Trokendi XR JDMF) empowers Trokendi XR 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 Trokendi XR JDMF during the approval evaluation for pharmaceutical products. At the time of Trokendi XR 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 Trokendi XR suppliers with JDMF on PharmaCompass.
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