01 2Fujian Fukang Pharmaceutical Co. , Ltd.
02 2JEIL PHARMACEUTICAL CO. , LTD.
03 1JW Pharmaceutical Corporation
04 2Kyongbo Pharmaceutical Co. , Ltd.
05 1Yungjin Pharm. Co. ,Ltd
01 1Cefmetazole Sodium
02 4Cefmetazole sodium
03 1Cefmethazole sodium
04 1Japanese Pharmacopoeia cefmetazole sodium
05 1Japanese Pharmacopoeia cefmethazole sodium (sterile)
01 2China
02 6South Korea
Registration Number : 229MF10047
Registrant's Address : No. 6, Gaogang Avenue, Jiangyin Industrial Estate, Fuqing, Fuzhou, Fujian, China
Initial Date of Registration : 2017-02-22
Latest Date of Registration : 2017-06-30
Registration Number : 306MF10072
Registrant's Address : No. 6, Gaogang Avenue, Jiangyin Industrial Estate, Fuqing, Fuzhou, Fujian, China
Initial Date of Registration : 2024-05-29
Latest Date of Registration : 2024-05-29
Registration Number : 223MF10135
Registrant's Address : 745-5, Banpo-dong, Seocho-ku, Seoul, Korea
Initial Date of Registration : 2011-08-19
Latest Date of Registration : 2011-08-19
Japanese Pharmacopoeia Cefmetazole Sodium
Registration Number : 223MF10099
Registrant's Address : 343, Sapyeong-daero, Seocho-gu, Seoul, Korea
Initial Date of Registration : 2011-07-11
Latest Date of Registration : 2011-07-11
Registration Number : 220MF10186
Registrant's Address : 2477, Nambusunhwan-ro Seocho-gu, Seoul, Republic of Korea
Initial Date of Registration : 2008-07-31
Latest Date of Registration : 2008-07-31
Japanese Pharmacopoeia Cefmetazole Sodium (Sterile)
Registration Number : 304MF10008
Registrant's Address : 174, Sirok-ro, Asan-si, Chungcheongnam-do, KOREA
Initial Date of Registration : 2022-01-11
Latest Date of Registration : 2022-01-11
Registration Number : 303MF10160
Registrant's Address : 174, Sirok-ro, Asan-si, Chungcheongnam-do, KOREA
Initial Date of Registration : 2021-10-21
Latest Date of Registration : 2021-10-21
Registration Number : 220MF10102
Registrant's Address : 13, Olympic-ro 35da-gil, Songpa-gu, Seoul, Korea
Initial Date of Registration : 2008-04-11
Latest Date of Registration : 2014-09-01
66
PharmaCompass offers a list of Cefmetazole Sodium 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 Cefmetazole Sodium manufacturer or Cefmetazole Sodium supplier for your needs.
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PharmaCompass also assists you with knowing the Cefmetazole Sodium API Price utilized in the formulation of products. Cefmetazole Sodium API Price is not always fixed or binding as the Cefmetazole Sodium Price is obtained through a variety of data sources. The Cefmetazole Sodium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A LP00266 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of LP00266, including repackagers and relabelers. The FDA regulates LP00266 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. LP00266 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 LP00266 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A LP00266 supplier is an individual or a company that provides LP00266 active pharmaceutical ingredient (API) or LP00266 finished formulations upon request. The LP00266 suppliers may include LP00266 API manufacturers, exporters, distributors and traders.
click here to find a list of LP00266 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 LP00266 Drug Master File in Japan (LP00266 JDMF) empowers LP00266 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 LP00266 JDMF during the approval evaluation for pharmaceutical products. At the time of LP00266 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 LP00266 suppliers with JDMF on PharmaCompass.
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