01 1Hamari PFST Co., Ltd.
02 1ILDONG PHARMACEUTICAL CO. , LTD.
03 1Johko Pharmaceutical Co., Ltd.
04 1Kongo Chemical Co., Ltd.
05 3Mikuni Pharmaceutical Co., Ltd.
01 1Furusuruchiamin hydrochloride "production-only"
02 1Hydrochloric acid Furusuruchiamin (production only)
03 3Japanese Pharmacopoeia Furusuruchiamin hydrochloride (production only)
04 1Japanese Pharmacopoeia hydrochloric acid Furusuruchiamin (production only)
05 1Outsiders regulations Furusuruchiamin (production only)
01 6Japan
02 1South Korea
Fursultiamine hydrochloride (for manufacturing purposes only)
Registration Number : 225MF10177
Registrant's Address : 2. Baumoe-ro 27-gil, Seocho-gu, Seoul, Korea
Initial Date of Registration : 2013-09-18
Latest Date of Registration : 2013-09-18
Fursultiamine hydrochloride (for manufacturing only)
Registration Number : 217MF11203
Registrant's Address : 3 Himata, Toyama City, Toyama Prefecture
Initial Date of Registration : 2005-12-12
Latest Date of Registration : 2007-05-02
Japanese Pharmacopoeia Fursultiamine Hydrochloride (for manufacturing only)
Registration Number : 218MF10915
Registrant's Address : 2-35 Shinshu-cho, Toyonaka City, Osaka Prefecture
Initial Date of Registration : 2006-11-21
Latest Date of Registration : 2006-11-21
Japanese Pharmacopoeia Fursultiamine Hydrochloride (for manufacturing only)
Registration Number : 218MF11035
Registrant's Address : 2-35 Shinshu-cho, Toyonaka City, Osaka Prefecture
Initial Date of Registration : 2006-12-28
Latest Date of Registration : 2006-12-28
Extra-official regulations Fursultiamine (for manufacturing only)
Registration Number : 221MF10037
Registrant's Address : 2-35 Shinshu-cho, Toyonaka City, Osaka Prefecture
Initial Date of Registration : 2009-02-09
Latest Date of Registration : 2009-02-09
Japanese Pharmacopoeia Fursultiamine Hydrochloride (For manufacturing only)
Registration Number : 218MF10979
Registrant's Address : 5 Kajigaishi Nishi 1-chome, Kitanagoya City, Aichi Prefecture
Initial Date of Registration : 2006-12-01
Latest Date of Registration : 2006-12-01
Japanese Pharmacopoeia Fursultiamine Hydrochloride (for manufacturing only)
Registration Number : 217MF10856
Registrant's Address : Osaka Prefecture, Osaka City, Suminoe Ward, Nanko Kita 1-19-40
Initial Date of Registration : 2005-11-01
Latest Date of Registration : 2007-01-22
16
PharmaCompass offers a list of Fursultiamine 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 Fursultiamine manufacturer or Fursultiamine supplier for your needs.
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PharmaCompass also assists you with knowing the Fursultiamine API Price utilized in the formulation of products. Fursultiamine API Price is not always fixed or binding as the Fursultiamine Price is obtained through a variety of data sources. The Fursultiamine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A TTFD manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of TTFD, including repackagers and relabelers. The FDA regulates TTFD manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. TTFD 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 TTFD manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A TTFD supplier is an individual or a company that provides TTFD active pharmaceutical ingredient (API) or TTFD finished formulations upon request. The TTFD suppliers may include TTFD API manufacturers, exporters, distributors and traders.
click here to find a list of TTFD 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 TTFD Drug Master File in Japan (TTFD JDMF) empowers TTFD 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 TTFD JDMF during the approval evaluation for pharmaceutical products. At the time of TTFD 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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