01 1Chongqing Huapont Shengchem Pharm. Co. , Ltd.
02 1Chongqing Huapont Shengchem Pharmaceutical Co. , Ltd.
03 1HETERO DRUGS LIMITED.
04 1YiChang HEC ChangJiang Pharmaceutical Co. , Ltd.
05 3Zhejiang NHU Company Ltd.
01 4Moxifloxacin Hydrochloride
02 1Moxifloxacin Hydrochloride (Moxifloxacin HCl)
03 2Moxifloxacin hydrochloride
01 6China
02 1India
Registration Number : 307MF10131
Registrant's Address : No. 69 Xingguang Avenue, Renhe Town, Yubei District, Chongqing, China, 401121
Initial Date of Registration : 2025-10-29
Latest Date of Registration : 2025-10-29
Moxifloxacin Hydrochloride (Moxifloxacin HCl)
Registration Number : 230MF10171
Registrant's Address : No. 69 Xingguang Avenue, Renhe Town, Yubei District, Chongqing, China
Initial Date of Registration : 2018-12-21
Latest Date of Registration : 2018-12-21
Registration Number : 226MF10043
Registrant's Address : 7-2-A2, Hetero Corporate, Industrial Estates, Sanath Nagar, Hyderabad-500 018, Andhra...
Initial Date of Registration : 2014-02-19
Latest Date of Registration : 2014-02-19
Registration Number : 307MF10119
Registrant's Address : No. 38 Binjiang Road, Yidu, Hubei Province, P. R. China
Initial Date of Registration : 2025-09-26
Latest Date of Registration : 2025-09-26
Registration Number : 229MF10085
Registrant's Address : No. 4 Jiangbeiroad, Yulin street, Xinchang county, Zhejiang province, China
Initial Date of Registration : 2017-04-14
Latest Date of Registration : 2017-04-14
Registration Number : 305MF10093
Registrant's Address : No. 4 Jiangbeiroad, Yulin street, Xinchang county, Zhejiang province, China
Initial Date of Registration : 2023-08-02
Latest Date of Registration : 2023-08-02
Registration Number : 231MF10026
Registrant's Address : No. 4 Jiangbeiroad, Yulin street, Xinchang county, Zhejiang province, China
Initial Date of Registration : 2019-02-05
Latest Date of Registration : 2019-02-05
13
PharmaCompass offers a list of Moxifloxacin Hydrochloride 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 Moxifloxacin Hydrochloride manufacturer or Moxifloxacin Hydrochloride supplier for your needs.
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PharmaCompass also assists you with knowing the Moxifloxacin Hydrochloride API Price utilized in the formulation of products. Moxifloxacin Hydrochloride API Price is not always fixed or binding as the Moxifloxacin Hydrochloride Price is obtained through a variety of data sources. The Moxifloxacin Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Vigamox manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Vigamox, including repackagers and relabelers. The FDA regulates Vigamox manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Vigamox 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 Vigamox manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Vigamox supplier is an individual or a company that provides Vigamox active pharmaceutical ingredient (API) or Vigamox finished formulations upon request. The Vigamox suppliers may include Vigamox API manufacturers, exporters, distributors and traders.
click here to find a list of Vigamox 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 Vigamox Drug Master File in Japan (Vigamox JDMF) empowers Vigamox 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 Vigamox JDMF during the approval evaluation for pharmaceutical products. At the time of Vigamox 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 Vigamox suppliers with JDMF on PharmaCompass.
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