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...
85
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A 93350_SIGMA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 93350_SIGMA, including repackagers and relabelers. The FDA regulates 93350_SIGMA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 93350_SIGMA 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 93350_SIGMA manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A 93350_SIGMA supplier is an individual or a company that provides 93350_SIGMA active pharmaceutical ingredient (API) or 93350_SIGMA finished formulations upon request. The 93350_SIGMA suppliers may include 93350_SIGMA 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 93350_SIGMA Drug Master File in Korea (93350_SIGMA KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of 93350_SIGMA. The MFDS reviews the 93350_SIGMA KDMF as part of the drug registration process and uses the information provided in the 93350_SIGMA KDMF to evaluate the safety and efficacy of the drug.
After submitting a 93350_SIGMA 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 93350_SIGMA API can apply through the Korea Drug Master File (KDMF).
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