01 1Daito Co., Ltd.
02 2FDC LIMITED.
03 1GMFC LABS PVT LTD
04 1Hy-Gro Chemicals Pharmatek Private Limited.
05 1Hy-Gro Chemicals Pharmtek Private Limited
06 3KOLON LIFE SCIENCE, INC.
07 1PHARMARON MANUFACTURING SERVICES (UK) LTD.
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PharmaCompass offers a list of Flurbiprofen 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 Flurbiprofen manufacturer or Flurbiprofen supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Flurbiprofen manufacturer or Flurbiprofen supplier.
PharmaCompass also assists you with knowing the Flurbiprofen API Price utilized in the formulation of products. Flurbiprofen API Price is not always fixed or binding as the Flurbiprofen Price is obtained through a variety of data sources. The Flurbiprofen Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A C07013 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of C07013, including repackagers and relabelers. The FDA regulates C07013 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. C07013 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 C07013 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A C07013 supplier is an individual or a company that provides C07013 active pharmaceutical ingredient (API) or C07013 finished formulations upon request. The C07013 suppliers may include C07013 API manufacturers, exporters, distributors and traders.
click here to find a list of C07013 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 C07013 Drug Master File in Japan (C07013 JDMF) empowers C07013 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 C07013 JDMF during the approval evaluation for pharmaceutical products. At the time of C07013 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 C07013 suppliers with JDMF on PharmaCompass.
We have 7 companies offering C07013
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