01 1Glaxo Wellcome Manufacturing Pte Ltd@[micronization process manufacturing company] Glaxo Operations UK Ltd
02 1Melody Healthcare Pvt. Ltd
01 1G-Max Pharmachem Co., Ltd.
02 1GlaxoSmithKline Inc.
01 1Villanterol triphenatate (micronized)
02 1Villanterol triphenate
01 1India
02 1United Kingdom
Registrant Name : GlaxoSmithKline Inc.
Registration Date : 2014-06-30
Registration Number : Su2480-12-ND
Manufacturer Name : Glaxo Wellcome Manufacturing...
Manufacturer Address : 1 Pioneer Sector 1, Singapore 628413@Priory Street, Ware, Hertfordshire, SG12 0DJ, Un...
Villanterol triphenatate (micronized)
Registrant Name : G-Max Pharmachem Co., Ltd.
Registration Date : 2025-10-02
Registration Number : Su660-1-ND
Manufacturer Name : Melody Healthcare Pvt. Ltd
Manufacturer Address : Plot No. J-73, MIDC, Tarapur, Boisar Dist. Palghar – 401 506, Maharashtra State, In...
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PharmaCompass offers a list of Vilanterol Trifenatate 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 Vilanterol Trifenatate manufacturer or Vilanterol Trifenatate supplier for your needs.
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PharmaCompass also assists you with knowing the Vilanterol Trifenatate API Price utilized in the formulation of products. Vilanterol Trifenatate API Price is not always fixed or binding as the Vilanterol Trifenatate Price is obtained through a variety of data sources. The Vilanterol Trifenatate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A BREO ELLIPTA-1 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of BREO ELLIPTA-1, including repackagers and relabelers. The FDA regulates BREO ELLIPTA-1 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. BREO ELLIPTA-1 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 BREO ELLIPTA-1 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A BREO ELLIPTA-1 supplier is an individual or a company that provides BREO ELLIPTA-1 active pharmaceutical ingredient (API) or BREO ELLIPTA-1 finished formulations upon request. The BREO ELLIPTA-1 suppliers may include BREO ELLIPTA-1 API manufacturers, exporters, distributors and traders.
click here to find a list of BREO ELLIPTA-1 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 BREO ELLIPTA-1 Drug Master File in Korea (BREO ELLIPTA-1 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of BREO ELLIPTA-1. The MFDS reviews the BREO ELLIPTA-1 KDMF as part of the drug registration process and uses the information provided in the BREO ELLIPTA-1 KDMF to evaluate the safety and efficacy of the drug.
After submitting a BREO ELLIPTA-1 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 BREO ELLIPTA-1 API can apply through the Korea Drug Master File (KDMF).
click here to find a list of BREO ELLIPTA-1 suppliers with KDMF on PharmaCompass.
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