01 1Alfresa Fine Chemicals Co., Ltd.
02 1Assia Chemical Industries Ltd.
03 1DONGBANG FUTURE TECH & LIFE CO. , LTD.
04 2KOLON LIFE SCIENCE, INC.
05 1Permakem Asia Co., Ltd.
06 1Ranbaxy Laboratories Limited.
07 2YUHAN CORPORATION
08 2Zhejiang Starry Pharmaceutical Co. ,Ltd
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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, Price,and more, enabling you to easily find the right Levofloxacin manufacturer or Levofloxacin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Levofloxacin manufacturer or Levofloxacin supplier.
PharmaCompass also assists you with knowing the Levofloxacin API Price utilized in the formulation of products. Levofloxacin API Price is not always fixed or binding as the Levofloxacin Price is obtained through a variety of data sources. The Levofloxacin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Iquix manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Iquix, including repackagers and relabelers. The FDA regulates Iquix manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Iquix 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 Iquix manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Iquix supplier is an individual or a company that provides Iquix active pharmaceutical ingredient (API) or Iquix finished formulations upon request. The Iquix suppliers may include Iquix API manufacturers, exporters, distributors and traders.
click here to find a list of Iquix 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 Iquix Drug Master File in Japan (Iquix JDMF) empowers Iquix 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 Iquix JDMF during the approval evaluation for pharmaceutical products. At the time of Iquix 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 Iquix suppliers with JDMF on PharmaCompass.
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