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, Price,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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PharmaCompass also assists you with knowing the Mono Propylene Glycol API Price utilized in the formulation of products. Mono Propylene Glycol API Price is not always fixed or binding as the Mono Propylene Glycol Price is obtained through a variety of data sources. The Mono Propylene Glycol Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 57-55-6 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 57-55-6, including repackagers and relabelers. The FDA regulates 57-55-6 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 57-55-6 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 57-55-6 supplier is an individual or a company that provides 57-55-6 active pharmaceutical ingredient (API) or 57-55-6 finished formulations upon request. The 57-55-6 suppliers may include 57-55-6 API manufacturers, exporters, distributors and traders.
click here to find a list of 57-55-6 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 57-55-6 Drug Master File in Japan (57-55-6 JDMF) empowers 57-55-6 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 57-55-6 JDMF during the approval evaluation for pharmaceutical products. At the time of 57-55-6 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 57-55-6 suppliers with JDMF on PharmaCompass.
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