Farmak works in the development, production and marketing of APIs, Intermediates & Specialties// FDA inspected.
01 1FARMAK, a. s.
02 2Active Pharma Inc.
03 2Permakem Asia Co., Ltd.
04 1Ryoto Fine Co., Ltd.
01 1Japanese Pharmacopoeia tizanidine hydrochloride (production only)
02 2Tizanidine Hydrochloride
03 2Tizanidine hydrochloride
04 1Tizanidine hydrochloride (production only)
01 1Czech Republic
02 5Japan
Farmak works in the development, production and marketing of APIs, Intermediates & Specialties// FDA inspected.
Tizanidine hydrochloride (for manufacturing purposes only)
Registration Number : 227MF10142
Registrant's Address : Na vlcinci 16/3 Klasterni Hradisko 779 00 Olomouc Czech Republic
Initial Date of Registration : 2015-05-20
Latest Date of Registration : 2022-06-15
Registration Number : 303MF10146
Registrant's Address : 2-36-1 Kanda Jinbocho, Chiyoda-ku, Tokyo
Initial Date of Registration : 2021-09-09
Latest Date of Registration : 2021-09-09
Registration Number : 305MF10008
Registrant's Address : 1-10-11, Nihonbashi Horidomecho, Chuo-ku, Tokyo
Initial Date of Registration : 2023-01-18
Latest Date of Registration : 2023-01-18
Registration Number : 217MF10718
Registrant's Address : 1-10-11, Nihonbashi Horidomecho, Chuo-ku, Tokyo
Initial Date of Registration : 2005-10-07
Latest Date of Registration : 2010-02-16
Japanese Pharmacopoeia Tizanidine Hydrochloride (for manufacturing only)
Registration Number : 222MF10064
Registrant's Address : 1410 Takada, Kashiwa City, Chiba Prefecture
Initial Date of Registration : 2010-02-22
Latest Date of Registration : 2010-02-22
Registration Number : 218MF10572
Registrant's Address : 2-36-1 Kanda Jinbocho, Chiyoda-ku, Tokyo
Initial Date of Registration : 2006-06-15
Latest Date of Registration : 2006-06-15
A Tizanidin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tizanidin, including repackagers and relabelers. The FDA regulates Tizanidin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tizanidin 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 Tizanidin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tizanidin supplier is an individual or a company that provides Tizanidin active pharmaceutical ingredient (API) or Tizanidin finished formulations upon request. The Tizanidin suppliers may include Tizanidin API manufacturers, exporters, distributors and traders.
click here to find a list of Tizanidin 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 Tizanidin Drug Master File in Japan (Tizanidin JDMF) empowers Tizanidin 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 Tizanidin JDMF during the approval evaluation for pharmaceutical products. At the time of Tizanidin 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 Tizanidin suppliers with JDMF on PharmaCompass.
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