01 1Glaxo Wellcome Manufacturing Pte Ltd@[Pulverization Process Manufacturing Company]Glaxo Operations UK Limited (trading as Glaxo Wellcome Operations)
01 1GlaxoSmithKline Inc.
01 1Fluticasone furoate
01 1United Kingdom
Registrant Name : GlaxoSmithKline Inc.
Registration Date : 2008-05-07
Registration Number : 89-5-ND
Manufacturer Name : Glaxo Wellcome Manufacturing...
Manufacturer Address : 1 Pioneer Sector 1, Singapore 628413@[Micronization Process Manufacturer]Priory Stree...
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.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Fluticasone Furoate Drug Master File in Korea (Fluticasone Furoate KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Fluticasone Furoate. The MFDS reviews the Fluticasone Furoate KDMF as part of the drug registration process and uses the information provided in the Fluticasone Furoate KDMF to evaluate the safety and efficacy of the drug.
After submitting a Fluticasone Furoate 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 Fluticasone Furoate API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Fluticasone Furoate suppliers with KDMF on PharmaCompass.
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