01 1FORMOSA LABORATORIES, INC.
02 1Kyongbo Pharmaceutical Co. , Ltd.
03 1Shiratori Pharmaceutical Co., Ltd.
04 1Sumitomo Chemical Co., Ltd.
01 3Oteracil potassium
02 1Oteracil potassium production dedicated
01 2Japan
02 1South Korea
03 1Taiwan
Registration Number : 224MF10134
Registrant's Address : 36 Hoping Street, Louchu, Taoyuan 33842, Taiwan
Initial Date of Registration : 2012-07-19
Latest Date of Registration : 2013-05-22
Registration Number : 224MF10034
Registrant's Address : 174, Sirok-ro, Asan-si, Chungcheongnam-do, KOREA
Initial Date of Registration : 2012-02-15
Latest Date of Registration : 2012-02-15
Oteracil Potassium For manufacturing only
Registration Number : 225MF10004
Registrant's Address : 6-11-24 Tsudanuma, Narashino City, Chiba Prefecture
Initial Date of Registration : 2013-01-18
Latest Date of Registration : 2013-01-18
Registration Number : 219MF10375
Registrant's Address : 2-7-1 Nihonbashi, Chuo-ku, Tokyo
Initial Date of Registration : 2007-12-19
Latest Date of Registration : 2007-12-19
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PharmaCompass offers a list of Oteracil Potassium 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 Oteracil Potassium manufacturer or Oteracil Potassium supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Oteracil Potassium manufacturer or Oteracil Potassium supplier.
PharmaCompass also assists you with knowing the Oteracil Potassium API Price utilized in the formulation of products. Oteracil Potassium API Price is not always fixed or binding as the Oteracil Potassium Price is obtained through a variety of data sources. The Oteracil Potassium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A KOX manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of KOX, including repackagers and relabelers. The FDA regulates KOX manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. KOX 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 KOX manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A KOX supplier is an individual or a company that provides KOX active pharmaceutical ingredient (API) or KOX finished formulations upon request. The KOX suppliers may include KOX API manufacturers, exporters, distributors and traders.
click here to find a list of KOX 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 KOX Drug Master File in Japan (KOX JDMF) empowers KOX 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 KOX JDMF during the approval evaluation for pharmaceutical products. At the time of KOX 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 KOX suppliers with JDMF on PharmaCompass.
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