EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
01 1EUROAPI FRANCE
02 1Wavelength Enterprises Ltd
03 1Alps Pharmaceutical Co., Ltd.
04 1Aurisco Pharmaceutical Co. , Ltd.
05 1HOVIONE FARMACIENCIA SA
06 1Sterling S. p. A.
01 3Fluticasone Propionate
02 3Fluticasone propionate
01 1China
02 2France
03 1Italy
04 1Japan
05 1Portugal
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
Registration Number : 303MF10172
Registrant's Address : 15 rue Traversie(')re 75012 Paris France
Initial Date of Registration : 2021-12-09
Latest Date of Registration : 2021-12-09
Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients & provides custom-made solutions.
Registration Number : 218MF10834
Registrant's Address : Offer Park, Building C, 4th floor, 94 Shlomo Shmeltzer Road, POB 3158, Petah Tikva 49...
Initial Date of Registration : 2006-10-20
Latest Date of Registration : 2021-05-13
Registration Number : 224MF10093
Registrant's Address : 2-10-50 Mukaimachi, Furukawa-cho, Hida-shi, Gifu Prefecture
Initial Date of Registration : 2012-04-25
Latest Date of Registration : 2012-04-25
Registration Number : 302MF10118
Registrant's Address : Badu Industrial Park Zone, Tiantai, Zhejiang province, 317200, P. R. China
Initial Date of Registration : 2020-10-01
Latest Date of Registration : 2020-10-01
Registration Number : 223MF10176
Registrant's Address : Sete Casas 2674-506 Loures PORTUGAL
Initial Date of Registration : 2011-12-27
Latest Date of Registration : 2022-12-15
Registration Number : 222MF10142
Registrant's Address : Via Della Carboneria 30 Solomeo 06073 Corciano Perugia-Italy
Initial Date of Registration : 2010-04-20
Latest Date of Registration : 2020-10-01
A Flixotide Inhaler manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Flixotide Inhaler, including repackagers and relabelers. The FDA regulates Flixotide Inhaler manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Flixotide Inhaler 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 Flixotide Inhaler manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Flixotide Inhaler supplier is an individual or a company that provides Flixotide Inhaler active pharmaceutical ingredient (API) or Flixotide Inhaler finished formulations upon request. The Flixotide Inhaler suppliers may include Flixotide Inhaler API manufacturers, exporters, distributors and traders.
click here to find a list of Flixotide Inhaler 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 Flixotide Inhaler Drug Master File in Japan (Flixotide Inhaler JDMF) empowers Flixotide Inhaler 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 Flixotide Inhaler JDMF during the approval evaluation for pharmaceutical products. At the time of Flixotide Inhaler 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 Flixotide Inhaler suppliers with JDMF on PharmaCompass.
We have 6 companies offering Flixotide Inhaler
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