01 1ACS DOBFAR S. P. A.
02 1Yungjin Pharmaceutical Co. , LTD.
03 1Yungjin Pharmaceutical. Co. , Ltd.
01 1Cefatrizine Propylene Glycol
02 1Cefatrizine Propylene Glycolate
03 1Sepharose tolidine propylene glycol
01 1Italy
02 2South Korea
Registration Number : 218MF10590
Registrant's Address : VIALE ADDETTA, 6/8/10 20067 TRIBIANO (Milan) ITALY
Initial Date of Registration : 2006-06-22
Latest Date of Registration : 2006-06-22
Registration Number : 218MF10762
Registrant's Address : 451-20, Cheonho-dong, Gangdong-gu, Seoul, Korea
Initial Date of Registration : 2006-09-06
Latest Date of Registration : 2010-01-22
Cefatrizine Propylene Glycolate
Registration Number : 220MF10063
Registrant's Address : 451-20, Cheonho-dong, Gangdong-gu, Seoul, Korea
Initial Date of Registration : 2008-02-25
Latest Date of Registration : 2008-02-25
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PharmaCompass offers a list of Mono Propylene Glycol API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Mono Propylene Glycol manufacturer or Mono Propylene Glycol supplier for your needs.
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A General lube manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of General lube, including repackagers and relabelers. The FDA regulates General lube manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. General lube 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 General lube manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A General lube supplier is an individual or a company that provides General lube active pharmaceutical ingredient (API) or General lube finished formulations upon request. The General lube suppliers may include General lube API manufacturers, exporters, distributors and traders.
click here to find a list of General lube suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 General lube Drug Master File in Japan (General lube JDMF) empowers General lube 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 General lube JDMF during the approval evaluation for pharmaceutical products. At the time of General lube 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 General lube suppliers with JDMF on PharmaCompass.
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