01 1Alfresa Fine Chemical Co., Ltd.
02 1Assia Chemical Industries Ltd.
03 1DONGBANG FUTURE TECH & LIFE CO. , LTD.
04 2KOLON LIFE SCIENCE, INC.
05 1Permachem Asia Co., Ltd.
06 1Ranbaxy Laboratories Limited.
07 2YUHAN CORPORATION
08 2Zhejiang Starry Pharmaceutical Co. ,Ltd
01 8Levofloxacin
02 1Levofloxacin (N)
03 1Levofloxacin (Teva)
04 1Levofloxacin carboxylic acid ethyl ester
01 2China
02 1India
03 1Israel
04 2Japan
05 5South Korea
Registration Number : 217MF10956
Registrant's Address : 1-10-1 Mukaihama, Akita City, Akita Prefecture
Initial Date of Registration : 2005-11-14
Latest Date of Registration : 2007-04-27
Registration Number : 218MF10535
Registrant's Address : Neot-Hovav Eco-Industrial Park, Be'er Sheva 8412316, Israel
Initial Date of Registration : 2006-06-01
Latest Date of Registration : 2024-08-22
Registration Number : 222MF10053
Registrant's Address : 904-5, Sangsin ri, Hyangnam eup, Hwasung si, Kyonggi do, 445-922, Korea
Initial Date of Registration : 2010-02-12
Latest Date of Registration : 2010-02-12
Registration Number : 218MF10403
Registrant's Address : 110, MAGOKDONG-RO, GANGSEO-GU, SEOUL, KOREA
Initial Date of Registration : 2006-04-14
Latest Date of Registration : 2007-01-18
Registration Number : 224MF10104
Registrant's Address : 110, MAGOKDONG-RO, GANGSEO-GU, SEOUL, KOREA
Initial Date of Registration : 2012-06-22
Latest Date of Registration : 2014-12-26
Registration Number : 218MF10264
Registrant's Address : 1-10-11 Nihonbashi Horidomecho, Chuo-ku, Tokyo
Initial Date of Registration : 2006-02-17
Latest Date of Registration : 2007-01-18
Registration Number : 228MF10150
Registrant's Address : 74 Noryangjin-ro, Dongjak-gu, Seoul, Korea
Initial Date of Registration : 2016-08-08
Latest Date of Registration : 2016-08-08
Registration Number : 218MF10467
Registrant's Address : 74 Noryangjin-ro, Dongjak-gu, Seoul, Korea
Initial Date of Registration : 2006-04-27
Latest Date of Registration : 2014-09-01
Levofloxacin carboxylate ethyl ester
Registration Number : 229MF10188
Registrant's Address : No. 1 Starry Road of Xianju Modern Industrial Centralization Zone, Xianju, Zhejiang, ...
Initial Date of Registration : 2017-10-20
Latest Date of Registration : 2017-10-20
Registration Number : 219MF10109
Registrant's Address : No. 1 Starry Road of Xianju Modern Industrial Centralization Zone, Xianju, Zhejiang, ...
Initial Date of Registration : 2007-03-23
Latest Date of Registration : 2010-11-15
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PharmaCompass offers a list of Levofloxacin API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Levofloxacin manufacturer or Levofloxacin supplier for your needs.
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A Aeroquin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Aeroquin, including repackagers and relabelers. The FDA regulates Aeroquin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Aeroquin 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 Aeroquin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Aeroquin supplier is an individual or a company that provides Aeroquin active pharmaceutical ingredient (API) or Aeroquin finished formulations upon request. The Aeroquin suppliers may include Aeroquin API manufacturers, exporters, distributors and traders.
click here to find a list of Aeroquin suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 Aeroquin Drug Master File in Japan (Aeroquin JDMF) empowers Aeroquin 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 Aeroquin JDMF during the approval evaluation for pharmaceutical products. At the time of Aeroquin 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 Aeroquin suppliers with JDMF on PharmaCompass.
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