01 1LEO Pharma A/S
01 1Fusidic acid sodium
01 1Denmark
Registration Number : 218MF10952
Registrant's Address : Industryparken 55, DK-2750 Ballerup
Initial Date of Registration : 2006-11-24
Latest Date of Registration : 2019-09-26
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PharmaCompass offers a list of Sodium Fusidate 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 Sodium Fusidate manufacturer or Sodium Fusidate supplier for your needs.
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PharmaCompass also assists you with knowing the Sodium Fusidate API Price utilized in the formulation of products. Sodium Fusidate API Price is not always fixed or binding as the Sodium Fusidate Price is obtained through a variety of data sources. The Sodium Fusidate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Fucidina manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fucidina, including repackagers and relabelers. The FDA regulates Fucidina manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fucidina 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 Fucidina manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Fucidina supplier is an individual or a company that provides Fucidina active pharmaceutical ingredient (API) or Fucidina finished formulations upon request. The Fucidina suppliers may include Fucidina API manufacturers, exporters, distributors and traders.
click here to find a list of Fucidina 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 Fucidina Drug Master File in Japan (Fucidina JDMF) empowers Fucidina 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 Fucidina JDMF during the approval evaluation for pharmaceutical products. At the time of Fucidina 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 Fucidina suppliers with JDMF on PharmaCompass.
