EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
01 1Euroapi France
02 1Hovione FarmaCiencia SA
01 1Korea Mundipharma Co., Ltd.
02 1Synex Co., Ltd.
01 2Micronized fluticasone propionate
01 1France
02 1Portugal
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
Micronized fluticasone propionate
Registrant Name : Korea Mundipharma Co., Ltd.
Registration Date : 2024-05-31
Registration Number : 20240531-209-J-1652
Manufacturer Name : Euroapi France
Manufacturer Address : 4 Lieu Dit La Paterie, Vertolaye, 63480, France
Micronized fluticasone propionate
Registrant Name : Synex Co., Ltd.
Registration Date : 2021-03-25
Registration Number : 20210325-209-J-917
Manufacturer Name : Hovione FarmaCiencia SA
Manufacturer Address : Sete Casas, Loures, 2674-506 Portugal
24
PharmaCompass offers a list of Fluticasone Propionate 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 Fluticasone Propionate manufacturer or Fluticasone Propionate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Fluticasone Propionate manufacturer or Fluticasone Propionate supplier.
PharmaCompass also assists you with knowing the Fluticasone Propionate API Price utilized in the formulation of products. Fluticasone Propionate API Price is not always fixed or binding as the Fluticasone Propionate Price is obtained through a variety of data sources. The Fluticasone Propionate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Flovent HFA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Flovent HFA, including repackagers and relabelers. The FDA regulates Flovent HFA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Flovent HFA 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 Flovent HFA manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Flovent HFA supplier is an individual or a company that provides Flovent HFA active pharmaceutical ingredient (API) or Flovent HFA finished formulations upon request. The Flovent HFA suppliers may include Flovent HFA API manufacturers, exporters, distributors and traders.
click here to find a list of Flovent HFA suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Flovent HFA Drug Master File in Korea (Flovent HFA KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Flovent HFA. The MFDS reviews the Flovent HFA KDMF as part of the drug registration process and uses the information provided in the Flovent HFA KDMF to evaluate the safety and efficacy of the drug.
After submitting a Flovent HFA KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their Flovent HFA API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Flovent HFA suppliers with KDMF on PharmaCompass.
