01 2Yoshindo Co., Ltd.
02 1Zhejiang Lepu Pharmaceutical Co. , Ltd.
01 1Day stations norfloxacin (production only)
02 1Norfloxacin
03 1Norfloxacin (N)
01 1China
02 2Japan
Registration Number : 225MF10086
Registrant's Address : 3697-8 Hagishima, Funamachi, Toyama City, Toyama Prefecture
Initial Date of Registration : 2013-04-23
Latest Date of Registration : 2013-04-23
JP Norfloxacin (for manufacturing purposes only)
Registration Number : 218MF10448
Registrant's Address : 3697-8 Hagishima, Funamachi, Toyama City, Toyama Prefecture
Initial Date of Registration : 2006-04-27
Latest Date of Registration : 2007-12-19
Registration Number : 226MF10208
Registrant's Address : No. 29 Binhai Road, Jiaojiang District, Taizhou City, Zhejiang Province, 318000, Chin...
Initial Date of Registration : 2014-10-27
Latest Date of Registration : 2014-10-27
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PharmaCompass offers a list of Norfloxacin 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 Norfloxacin manufacturer or Norfloxacin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Norfloxacin manufacturer or Norfloxacin supplier.
PharmaCompass also assists you with knowing the Norfloxacin API Price utilized in the formulation of products. Norfloxacin API Price is not always fixed or binding as the Norfloxacin Price is obtained through a variety of data sources. The Norfloxacin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A AM 715 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of AM 715, including repackagers and relabelers. The FDA regulates AM 715 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. AM 715 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 AM 715 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A AM 715 supplier is an individual or a company that provides AM 715 active pharmaceutical ingredient (API) or AM 715 finished formulations upon request. The AM 715 suppliers may include AM 715 API manufacturers, exporters, distributors and traders.
click here to find a list of AM 715 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 AM 715 Drug Master File in Japan (AM 715 JDMF) empowers AM 715 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 AM 715 JDMF during the approval evaluation for pharmaceutical products. At the time of AM 715 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 AM 715 suppliers with JDMF on PharmaCompass.
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