01 1ACS DOBFAR S. p. A.
02 1Antibiotics S. A. Leon Factory
03 1LUPIN LIMITED.
04 1Yungjin Pharmaceutical Co. , LTD.
01 4Cephalexin
01 1India
02 1Italy
03 1South Korea
04 1Spain
Registration Number : 218MF10523
Registrant's Address : Viale Addetta, 4/12, 20067 Tribiano (Milan) Italy
Initial Date of Registration : 2006-05-18
Latest Date of Registration : 2018-04-17
Registration Number : 220MF10148
Registrant's Address : Avenida de Antibioticos 59/61 24009 Leon, Spain
Initial Date of Registration : 2008-06-10
Latest Date of Registration : 2008-06-10
Registration Number : 302MF10062
Registrant's Address : Kalpataru Inspire, 3rd Floor, Off Western Express Highway, Santacruz (East), Mumbai 4...
Initial Date of Registration : 2020-05-29
Latest Date of Registration : 2020-05-29
Registration Number : 220MF10062
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 Cephalexin 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 Cephalexin manufacturer or Cephalexin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Cephalexin manufacturer or Cephalexin supplier.
PharmaCompass also assists you with knowing the Cephalexin API Price utilized in the formulation of products. Cephalexin API Price is not always fixed or binding as the Cephalexin Price is obtained through a variety of data sources. The Cephalexin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A CEX manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CEX, including repackagers and relabelers. The FDA regulates CEX manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CEX 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 CEX manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A CEX supplier is an individual or a company that provides CEX active pharmaceutical ingredient (API) or CEX finished formulations upon request. The CEX suppliers may include CEX API manufacturers, exporters, distributors and traders.
click here to find a list of CEX 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 CEX Drug Master File in Japan (CEX JDMF) empowers CEX 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 CEX JDMF during the approval evaluation for pharmaceutical products. At the time of CEX 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 CEX suppliers with JDMF on PharmaCompass.
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