01 1Titan Pharmaceutical Co. , Ltd.
01 1Cefuroxime Axetil
01 1Blank
Registration Number : 307MF10120
Registrant's Address : Lantang Town, Zijin County, Heyuan City, Guangdong Province, China
Initial Date of Registration : 2025-10-03
Latest Date of Registration : 2025-10-03
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PharmaCompass offers a list of Cefuroxime Axetil 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 Cefuroxime Axetil manufacturer or Cefuroxime Axetil supplier for your needs.
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PharmaCompass also assists you with knowing the Cefuroxime Axetil API Price utilized in the formulation of products. Cefuroxime Axetil API Price is not always fixed or binding as the Cefuroxime Axetil Price is obtained through a variety of data sources. The Cefuroxime Axetil Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Cefuroxime manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cefuroxime, including repackagers and relabelers. The FDA regulates Cefuroxime manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cefuroxime 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 Cefuroxime supplier is an individual or a company that provides Cefuroxime active pharmaceutical ingredient (API) or Cefuroxime finished formulations upon request. The Cefuroxime suppliers may include Cefuroxime API manufacturers, exporters, distributors and traders.
click here to find a list of Cefuroxime 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 Cefuroxime Drug Master File in Japan (Cefuroxime JDMF) empowers Cefuroxime 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 Cefuroxime JDMF during the approval evaluation for pharmaceutical products. At the time of Cefuroxime JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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