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