Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients & provides custom-made solutions.
01 1Wavelength Enterprises Ltd
02 1INDUSTRIALE CHIMICA s. r. l.
01 1Fluticasone Furoate
02 1Fluticasone furancarboxylic acid ester
01 1France
02 1Italy
Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients & provides custom-made solutions.
Registration Number : 304MF10038
Registrant's Address : Offer Park, Building C, 4th floor, 94 Shlomo Shmeltzer Road, POB 3158, Petah Tikva 49...
Initial Date of Registration : 2022-02-17
Latest Date of Registration : 2022-02-17
Registration Number : 305MF10120
Registrant's Address : Via E. H. Grieg, 13,21047 Saronno (VARESE) ITALY
Initial Date of Registration : 2023-11-15
Latest Date of Registration : 2023-11-15
A Fluticasone Furoate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fluticasone Furoate, including repackagers and relabelers. The FDA regulates Fluticasone Furoate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fluticasone Furoate 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 Fluticasone Furoate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Fluticasone Furoate supplier is an individual or a company that provides Fluticasone Furoate active pharmaceutical ingredient (API) or Fluticasone Furoate finished formulations upon request. The Fluticasone Furoate suppliers may include Fluticasone Furoate API manufacturers, exporters, distributors and traders.
click here to find a list of Fluticasone Furoate 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 Fluticasone Furoate Drug Master File in Japan (Fluticasone Furoate JDMF) empowers Fluticasone Furoate 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 Fluticasone Furoate JDMF during the approval evaluation for pharmaceutical products. At the time of Fluticasone Furoate 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 Fluticasone Furoate suppliers with JDMF on PharmaCompass.
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