01 1Amicogen (China) Biopharm Co. , Ltd.
02 1HANMI FINE CHEMICAL CO. , LTD.
03 1Orchid Chemicals & Pharmaceuticals Limited
04 1Parabolic Drugs Ltd.
05 1Yungjin Pharm. Co. ,Ltd
06 1Zhejiang Apeloa Tospo Pharmaceutical Co. , Ltd.
01 6Cefdinir
01 2China
02 2India
03 2South Korea
Registration Number : 228MF10084
Registrant's Address : No. 1688 Shixian Road, Jining City, Shandong Province
Initial Date of Registration : 2016-04-06
Latest Date of Registration : 2016-04-06
Registration Number : 218MF10515
Registrant's Address : 57, Gyeongje-ro, Siheung-si, Gyeonggi-do, Korea
Initial Date of Registration : 2006-05-18
Latest Date of Registration : 2017-10-30
Registration Number : 223MF10020
Registrant's Address : Orchid Towers, 313, Valluvar Kottam High Road, Nungambakkam, Chennai-600 034 India
Initial Date of Registration : 2011-02-08
Latest Date of Registration : 2011-02-08
Registration Number : 228MF10044
Registrant's Address : S. C. O. 99-100, 3rd & 4th Floor, Sector 17-B, Chandigarh-160017, INDIA
Initial Date of Registration : 2016-02-08
Latest Date of Registration : 2016-02-08
Registration Number : 228MF10039
Registrant's Address : 13, Olympic-ro 35da-gil, Songpa-gu, Seoul, Korea
Initial Date of Registration : 2016-02-08
Latest Date of Registration : 2016-02-08
Registration Number : 230MF10109
Registrant's Address : No. 519 Jiangnan Road, Hengdian Industrial Zone, Dongyang City, Jinhua, Zhejiang Prov...
Initial Date of Registration : 2018-08-20
Latest Date of Registration : 2018-08-20
A Cefdinir manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cefdinir, including repackagers and relabelers. The FDA regulates Cefdinir manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cefdinir 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 Cefdinir manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cefdinir supplier is an individual or a company that provides Cefdinir active pharmaceutical ingredient (API) or Cefdinir finished formulations upon request. The Cefdinir suppliers may include Cefdinir API manufacturers, exporters, distributors and traders.
click here to find a list of Cefdinir 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 Cefdinir Drug Master File in Japan (Cefdinir JDMF) empowers Cefdinir 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 Cefdinir JDMF during the approval evaluation for pharmaceutical products. At the time of Cefdinir 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 Cefdinir suppliers with JDMF on PharmaCompass.
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