01 1Sam-O Pharmaceutical Co., Ltd.
01 1Sam-O Pharmaceutical Co., Ltd.
01 1Pelubiprofentromethamine (micronized)
01 1Uzbekistan
Pelubiprofentromethamine (micronized)
Registrant Name : Sam-O Pharmaceutical Co., Ltd.
Registration Date : 2020-08-05
Registration Number : 2105-44-ND
Manufacturer Name : Sam-O Pharmaceutical Co., Lt...
Manufacturer Address : 63, Okgucheonseo-ro 81beon-gil, Siheung-si, Gyeonggi-do (Room 705, Sihwa Industrial C...
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A 1606-EP2275420A1 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 1606-EP2275420A1, including repackagers and relabelers. The FDA regulates 1606-EP2275420A1 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 1606-EP2275420A1 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A 1606-EP2275420A1 supplier is an individual or a company that provides 1606-EP2275420A1 active pharmaceutical ingredient (API) or 1606-EP2275420A1 finished formulations upon request. The 1606-EP2275420A1 suppliers may include 1606-EP2275420A1 API manufacturers, exporters, distributors and traders.
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In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a 1606-EP2275420A1 Drug Master File in Korea (1606-EP2275420A1 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of 1606-EP2275420A1. The MFDS reviews the 1606-EP2275420A1 KDMF as part of the drug registration process and uses the information provided in the 1606-EP2275420A1 KDMF to evaluate the safety and efficacy of the drug.
After submitting a 1606-EP2275420A1 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 1606-EP2275420A1 API can apply through the Korea Drug Master File (KDMF).
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