01 1JEIL PHARMACEUTICAL CO. , LTD.
02 1Meiji Seika Pharma Co., Ltd.
03 2Yungjin Pharm. Co. ,Ltd
01 2Cefditoren Pivoxil
02 2Cefditoren pivoxil
01 1Japan
02 3South Korea
Registration Number : 219MF10254
Registrant's Address : 343, Sapyeong-daero, Seocho-gu, Seoul, Korea
Initial Date of Registration : 2007-08-06
Latest Date of Registration : 2007-08-06
Registration Number : 302MF10072
Registrant's Address : 2-4-16 Kyobashi, Chuo-ku, Tokyo
Initial Date of Registration : 2020-06-26
Latest Date of Registration : 2020-06-26
Registration Number : 306MF10127
Registrant's Address : 13, Olympic-ro 35da-gil, Songpa-gu, Seoul, Korea
Initial Date of Registration : 2024-09-18
Latest Date of Registration : 2024-09-18
Registration Number : 228MF10040
Registrant's Address : 13, Olympic-ro 35da-gil, Songpa-gu, Seoul, Korea
Initial Date of Registration : 2016-02-08
Latest Date of Registration : 2016-02-08
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PharmaCompass offers a list of Cefditoren Pivoxil 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 Cefditoren Pivoxil manufacturer or Cefditoren Pivoxil supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Cefditoren Pivoxil manufacturer or Cefditoren Pivoxil supplier.
PharmaCompass also assists you with knowing the Cefditoren Pivoxil API Price utilized in the formulation of products. Cefditoren Pivoxil API Price is not always fixed or binding as the Cefditoren Pivoxil Price is obtained through a variety of data sources. The Cefditoren Pivoxil Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A ME 1207 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of ME 1207, including repackagers and relabelers. The FDA regulates ME 1207 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. ME 1207 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 ME 1207 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A ME 1207 supplier is an individual or a company that provides ME 1207 active pharmaceutical ingredient (API) or ME 1207 finished formulations upon request. The ME 1207 suppliers may include ME 1207 API manufacturers, exporters, distributors and traders.
click here to find a list of ME 1207 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 ME 1207 Drug Master File in Japan (ME 1207 JDMF) empowers ME 1207 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 ME 1207 JDMF during the approval evaluation for pharmaceutical products. At the time of ME 1207 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 ME 1207 suppliers with JDMF on PharmaCompass.
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