Coral's API range includes Corticosteroids, Antihistamines. Hormones and Antineoplastics.
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01 1Coral Drugs Private Limited
02 1Glaxo Wellcome Manufacturing Pte Ltd@[Pulverization Process Manufacturing Company] Glaxo Operations UK Limited (trading as Glaxo Wellcome Operations)
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01 1Geonil Pharmaceutical Co., Ltd.
02 1GlaxoSmithKline Inc.
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01 1Fluticasone furoate
02 1Fluticasone furoate (micronized)
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01 1India
02 1United Kingdom
Fluticasone furoate (micronized)
Registrant Name : Geonil Pharmaceutical Co., Ltd.
Registration Date : 2025-02-14
Registration Number : Su458-6-ND
Manufacturer Name : Coral Drugs Private Limited
Manufacturer Address : 55-56-57, HSIIDC Industrial Estate, Murthal, Sonepat, Haryana 131039, India
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...
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PharmaCompass offers a list of Fluticasone Furoate 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 Furoate manufacturer or Fluticasone Furoate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Fluticasone Furoate manufacturer or Fluticasone Furoate supplier.
PharmaCompass also assists you with knowing the Fluticasone Furoate API Price utilized in the formulation of products. Fluticasone Furoate API Price is not always fixed or binding as the Fluticasone Furoate Price is obtained through a variety of data sources. The Fluticasone Furoate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A GSK 685 698 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of GSK 685 698, including repackagers and relabelers. The FDA regulates GSK 685 698 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. GSK 685 698 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 GSK 685 698 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A GSK 685 698 supplier is an individual or a company that provides GSK 685 698 active pharmaceutical ingredient (API) or GSK 685 698 finished formulations upon request. The GSK 685 698 suppliers may include GSK 685 698 API manufacturers, exporters, distributors and traders.
click here to find a list of GSK 685 698 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 GSK 685 698 Drug Master File in Korea (GSK 685 698 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of GSK 685 698. The MFDS reviews the GSK 685 698 KDMF as part of the drug registration process and uses the information provided in the GSK 685 698 KDMF to evaluate the safety and efficacy of the drug.
After submitting a GSK 685 698 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 GSK 685 698 API can apply through the Korea Drug Master File (KDMF).
click here to find a list of GSK 685 698 suppliers with KDMF on PharmaCompass.
We have 2 companies offering GSK 685 698
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