Centrient is a leading manufacturer of Beta-Lactam Antibiotics and a provider of next-generation Statins and Antifungals.
01 2Centrient Pharmaceuticals Spain S. A.
01 1Japanese Pharmacopoeia cephalexin
02 1Purilex (Cefalexin Monohydrate)
01 2Netherlands
Centrient is a leading manufacturer of Beta-Lactam Antibiotics and a provider of next-generation Statins and Antifungals.
Purilex (Cefalexin Monohydrate)
Registration Number : 304MF10144
Registrant's Address : C/ Ripolles 2, Santa Perpetua de Mogoda, 08130 Barcelona, Spain
Initial Date of Registration : 2022-10-26
Latest Date of Registration : 2025-02-07
Centrient is a leading manufacturer of Beta-Lactam Antibiotics and a provider of next-generation Statins and Antifungals.
Cephalexin, Japanese Pharmacopoeia
Registration Number : 218MF10199
Registrant's Address : C/ Ripolles 2, Santa Perpetua de Mogoda, 08130 Barcelona, Spain
Initial Date of Registration : 2006-02-08
Latest Date of Registration : 2025-02-07
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PharmaCompass offers a list of Cephalexin Monohydrate 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 Monohydrate manufacturer or Cephalexin Monohydrate supplier for your needs.
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PharmaCompass also assists you with knowing the Cephalexin Monohydrate API Price utilized in the formulation of products. Cephalexin Monohydrate API Price is not always fixed or binding as the Cephalexin Monohydrate Price is obtained through a variety of data sources. The Cephalexin Monohydrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Cefacet manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cefacet, including repackagers and relabelers. The FDA regulates Cefacet manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cefacet 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 Cefacet manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cefacet supplier is an individual or a company that provides Cefacet active pharmaceutical ingredient (API) or Cefacet finished formulations upon request. The Cefacet suppliers may include Cefacet API manufacturers, exporters, distributors and traders.
click here to find a list of Cefacet 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 Cefacet Drug Master File in Japan (Cefacet JDMF) empowers Cefacet 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 Cefacet JDMF during the approval evaluation for pharmaceutical products. At the time of Cefacet 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 Cefacet suppliers with JDMF on PharmaCompass.
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