01 1Glaxo Wellcome Manufacturing Pte Ltd@Catalent Micron Technologies Limited@Glaxo Operations UK Ltd (Trading as Glaxo Wellcome Operations)
01 1GlaxoSmithKline Inc.
01 1Cabotegravir sodium (micronized)
01 1United Kingdom
Cabotegravir sodium (micronized)
Registrant Name : GlaxoSmithKline Inc.
Registration Date : 2022-02-03
Registration Number : Su231-20-ND
Manufacturer Name : Glaxo Wellcome Manufacturing...
Manufacturer Address : 1 Pioneer Sector 1, 628413 Singapore@Crossways Boulevard, Crossways, Dartford, Kent, ...
A Cabotegravir Sodium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cabotegravir Sodium, including repackagers and relabelers. The FDA regulates Cabotegravir Sodium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cabotegravir Sodium 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 Cabotegravir Sodium manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cabotegravir Sodium supplier is an individual or a company that provides Cabotegravir Sodium active pharmaceutical ingredient (API) or Cabotegravir Sodium finished formulations upon request. The Cabotegravir Sodium suppliers may include Cabotegravir Sodium API manufacturers, exporters, distributors and traders.
click here to find a list of Cabotegravir Sodium 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 Cabotegravir Sodium Drug Master File in Korea (Cabotegravir Sodium KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Cabotegravir Sodium. The MFDS reviews the Cabotegravir Sodium KDMF as part of the drug registration process and uses the information provided in the Cabotegravir Sodium KDMF to evaluate the safety and efficacy of the drug.
After submitting a Cabotegravir Sodium 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 Cabotegravir Sodium API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Cabotegravir Sodium suppliers with KDMF on PharmaCompass.
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