01 1Nectar Lifesciences Ltd.
02 1Orchid Pharma Limited
03 1Parabolic Drugs Ltd.
04 1Qilu Antibiotics Pharmaceutical Co. , Ltd.
05 1Ranbaxy Laboratories Limited
06 1Sandoz GmbH
07 1Yungjin Pharm. Co. ,Ltd
01 2CEFPODOXIME PROXETIL
02 3Cefpodoxime Proxetil
03 2Cefpodoxime proxetil
01 1China
02 4India
03 1South Korea
04 1Switzerland
Registration Number : 301MF10023
Registrant's Address : Village Saidpura, Tehsil Dera Bassi, District Sahibzada Ajit Singh Nagar-140 507, Pun...
Initial Date of Registration : 2019-06-28
Latest Date of Registration : 2019-06-28
Registration Number : 306MF10078
Registrant's Address : Plot No. 121-128, 128A-133, 138-151, 159-164, SIDCO Industrial Estate, Alathur, Cheng...
Initial Date of Registration : 2024-06-12
Latest Date of Registration : 2024-06-12
Registration Number : 223MF10157
Registrant's Address : S. C. O. 99-100, 3rd & 4th Floor, Sector 17-B, Chandigarh-160017, INDIA
Initial Date of Registration : 2011-11-02
Latest Date of Registration : 2011-11-02
Registration Number : 303MF10058
Registrant's Address : No. 849 Dongjia Town, Licheng District, Jinan, Shandong, China
Initial Date of Registration : 2021-04-02
Latest Date of Registration : 2023-08-09
Registration Number : 222MF10026
Registrant's Address : Plot No. 90, Sector 32, Gurgaon, Haryana 122011, India
Initial Date of Registration : 2010-01-22
Latest Date of Registration : 2010-01-22
Registration Number : 225MF10129
Registrant's Address : Biochemiesstrasse 10,6250 Kundl, Austria
Initial Date of Registration : 2013-07-09
Latest Date of Registration : 2013-07-09
Registration Number : 227MF10122
Registrant's Address : 13, Olympic-ro 35da-gil, Songpa-gu, Seoul, Korea
Initial Date of Registration : 2015-04-22
Latest Date of Registration : 2015-04-22
A Cefpodoxime Proxetil manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cefpodoxime Proxetil, including repackagers and relabelers. The FDA regulates Cefpodoxime Proxetil manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cefpodoxime Proxetil 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 Cefpodoxime Proxetil manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cefpodoxime Proxetil supplier is an individual or a company that provides Cefpodoxime Proxetil active pharmaceutical ingredient (API) or Cefpodoxime Proxetil finished formulations upon request. The Cefpodoxime Proxetil suppliers may include Cefpodoxime Proxetil API manufacturers, exporters, distributors and traders.
click here to find a list of Cefpodoxime Proxetil 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 Cefpodoxime Proxetil Drug Master File in Japan (Cefpodoxime Proxetil JDMF) empowers Cefpodoxime Proxetil 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 Cefpodoxime Proxetil JDMF during the approval evaluation for pharmaceutical products. At the time of Cefpodoxime Proxetil 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 Cefpodoxime Proxetil suppliers with JDMF on PharmaCompass.
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