01 1Kyongbo Pharmaceutical Co. , Ltd.
02 1Orchid Chemicals & Pharmaceuticals Limited
03 1Qilu Antibiotics Pharmaceutical Co. , Ltd.
04 1Zhejiang Apeloa Tospo Pharmaceutical Co. , Ltd.
01 1Cefixime
02 1Cefixime Hydrate
03 2Cefixime hydrate
01 2China
02 1India
03 1South Korea
Registration Number : 224MF10092
Registrant's Address : 174, Sirok-ro, Asan-si, Chungcheongnam-do, KOREA
Initial Date of Registration : 2012-04-25
Latest Date of Registration : 2012-04-25
Registration Number : 222MF10120
Registrant's Address : Orchid Towers, 313, Valluvar Kottam High Road, Nungambakkam, Chennai-600 034 India
Initial Date of Registration : 2010-04-02
Latest Date of Registration : 2010-04-02
Registration Number : 226MF10199
Registrant's Address : No. 849 Dongjia Town, Licheng District, Jinan, Shandong, China
Initial Date of Registration : 2014-10-27
Latest Date of Registration : 2023-08-02
Registration Number : 302MF10060
Registrant's Address : No. 519 Jiangnan Road, Hengdian Industrial Zone, Dongyang City, Jinhua, Zhejiang Prov...
Initial Date of Registration : 2020-05-25
Latest Date of Registration : 2020-05-25
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PharmaCompass offers a list of Cefixime 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 Cefixime manufacturer or Cefixime supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Cefixime manufacturer or Cefixime supplier.
PharmaCompass also assists you with knowing the Cefixime API Price utilized in the formulation of products. Cefixime API Price is not always fixed or binding as the Cefixime Price is obtained through a variety of data sources. The Cefixime Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Cefiximum manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cefiximum, including repackagers and relabelers. The FDA regulates Cefiximum manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cefiximum 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 Cefiximum manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cefiximum supplier is an individual or a company that provides Cefiximum active pharmaceutical ingredient (API) or Cefiximum finished formulations upon request. The Cefiximum suppliers may include Cefiximum API manufacturers, exporters, distributors and traders.
click here to find a list of Cefiximum 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 Cefiximum Drug Master File in Japan (Cefiximum JDMF) empowers Cefiximum 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 Cefiximum JDMF during the approval evaluation for pharmaceutical products. At the time of Cefiximum 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 Cefiximum suppliers with JDMF on PharmaCompass.
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