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.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Mono Propylene Glycol manufacturer or Mono Propylene Glycol supplier.
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 (+-)-Propylene glycol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of (+-)-Propylene glycol, including repackagers and relabelers. The FDA regulates (+-)-Propylene glycol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. (+-)-Propylene glycol 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 (+-)-Propylene glycol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A (+-)-Propylene glycol supplier is an individual or a company that provides (+-)-Propylene glycol active pharmaceutical ingredient (API) or (+-)-Propylene glycol finished formulations upon request. The (+-)-Propylene glycol suppliers may include (+-)-Propylene glycol API manufacturers, exporters, distributors and traders.
click here to find a list of (+-)-Propylene glycol 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 (+-)-Propylene glycol Drug Master File in Japan ((+-)-Propylene glycol JDMF) empowers (+-)-Propylene glycol 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 (+-)-Propylene glycol JDMF during the approval evaluation for pharmaceutical products. At the time of (+-)-Propylene glycol 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 (+-)-Propylene glycol suppliers with JDMF on PharmaCompass.
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