01 1Glaxo Wellcome Manufacturing Pte. Ltd@[Micronized Manufacturing Plant]Catalent Micron Technologies Limited
02 1Shionogi Pharma Co., Ltd.@[Some process manufacturers] Fujimoto Chemicals Co., Ltd. Senboku Plant
01 2GlaxoSmithKline Inc.
01 1Dolutegravir sodium
02 1Dolutegravir sodium (micronized)
01 1Japan
02 1United Kingdom
Registrant Name : GlaxoSmithKline Inc.
Registration Date : 2020-08-13
Registration Number : Su231-19-ND
Manufacturer Name : Glaxo Wellcome Manufacturing...
Manufacturer Address : 1 Pioneer Sector 1, Singapore 628413@[Micronising Manufactory]Crossways Boulevard, Cr...
Dolutegravir sodium (micronized)
Registrant Name : GlaxoSmithKline Inc.
Registration Date : 2014-08-01
Registration Number : Su2480-14-ND
Manufacturer Name : Shionogi Pharma Co., Ltd.@[S...
Manufacturer Address : 224-20, Hiraishiebisuno, Kawauchi-cho, Tokushima, Tokushima 771-0132, Japan@1-24, Rin...
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PharmaCompass offers a list of Dolutegravir Sodium 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 Dolutegravir Sodium manufacturer or Dolutegravir Sodium supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Dolutegravir Sodium manufacturer or Dolutegravir Sodium supplier.
PharmaCompass also assists you with knowing the Dolutegravir Sodium API Price utilized in the formulation of products. Dolutegravir Sodium API Price is not always fixed or binding as the Dolutegravir Sodium Price is obtained through a variety of data sources. The Dolutegravir Sodium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A DLU manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DLU, including repackagers and relabelers. The FDA regulates DLU manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DLU 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 DLU manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A DLU supplier is an individual or a company that provides DLU active pharmaceutical ingredient (API) or DLU finished formulations upon request. The DLU suppliers may include DLU API manufacturers, exporters, distributors and traders.
click here to find a list of DLU 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 DLU Drug Master File in Korea (DLU KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of DLU. The MFDS reviews the DLU KDMF as part of the drug registration process and uses the information provided in the DLU KDMF to evaluate the safety and efficacy of the drug.
After submitting a DLU 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 DLU API can apply through the Korea Drug Master File (KDMF).
click here to find a list of DLU suppliers with KDMF on PharmaCompass.
