Farmak works in the development, production and marketing of APIs, Intermediates & Specialties// FDA inspected.
01 1FARMAK, a. s.
02 1MICRO LABS LIMITED.
03 1Piramal Pharma Limited
04 1Sanwa Chemical Co., Ltd.
01 2Brimonidine Tartrate
02 1Brimonidine tartrate
03 1Brimonidine tartrate (for manufacturing only)
01 1Czech Republic
02 1Hong Kong
03 2India
Farmak works in the development, production and marketing of APIs, Intermediates & Specialties// FDA inspected.
Registration Number : 302MF10029
Registrant's Address : Na vlcinci 16/3 Klasterni Hradisko 779 00 Olomouc Czech Republic
Initial Date of Registration : 2020-02-13
Latest Date of Registration : 2020-02-13
Registration Number : 301MF10111
Registrant's Address : 31, Race Course Road, Bengaluru-560 001, KARNATAKA, INDIA
Initial Date of Registration : 2019-12-20
Latest Date of Registration : 2019-12-20
Registration Number : 222MF10073
Registrant's Address : Digwal Village (Sy.Nos. 7-70, 70/1 and 70/2), Kohir Mandal, Sangareddy District-502 3...
Initial Date of Registration : 2010-02-25
Latest Date of Registration : 2011-11-01
Brimonidine Tartrate (for manufacturing purposes only)
Registration Number : 301MF10101
Registrant's Address : 24-8 Tamura 9-chome, Hiratsuka City, Kanagawa Prefecture
Initial Date of Registration : 2019-11-27
Latest Date of Registration : 2019-11-27
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A 59803-98-4 (Parent) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 59803-98-4 (Parent), including repackagers and relabelers. The FDA regulates 59803-98-4 (Parent) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 59803-98-4 (Parent) 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 59803-98-4 (Parent) supplier is an individual or a company that provides 59803-98-4 (Parent) active pharmaceutical ingredient (API) or 59803-98-4 (Parent) finished formulations upon request. The 59803-98-4 (Parent) suppliers may include 59803-98-4 (Parent) API manufacturers, exporters, distributors and traders.
click here to find a list of 59803-98-4 (Parent) 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 59803-98-4 (Parent) Drug Master File in Japan (59803-98-4 (Parent) JDMF) empowers 59803-98-4 (Parent) 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 59803-98-4 (Parent) JDMF during the approval evaluation for pharmaceutical products. At the time of 59803-98-4 (Parent) 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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