01 1Kyungdong Pharmaceutical Co., Ltd.
02 1Samhwa Biopharm Co., Ltd.
01 1Kyungdong Pharmaceutical Co., Ltd.
02 1Samhwa Biopharm Co., Ltd.
01 2Moniflumate
01 2South Korea
Registrant Name : Kyungdong Pharmaceutical Co., Ltd.
Registration Date : 2021-03-09
Registration Number : 20210309-211-J-859
Manufacturer Name : Kyungdong Pharmaceutical Co....
Manufacturer Address : 15, Balan Industrial Complex Road 2-gil, Hyangnam-eup, Hwaseong-si, Gyeonggi-do
Registrant Name : Samhwa Biopharm Co., Ltd.
Registration Date : 2019-12-03
Registration Number : 20191203-211-J-489
Manufacturer Name : Samhwa Biopharm Co., Ltd.
Manufacturer Address : 150 Hyeop-ro, Siheung-si, Gyeonggi-do
A Morniflumate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Morniflumate, including repackagers and relabelers. The FDA regulates Morniflumate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Morniflumate 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 Morniflumate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Morniflumate supplier is an individual or a company that provides Morniflumate active pharmaceutical ingredient (API) or Morniflumate finished formulations upon request. The Morniflumate suppliers may include Morniflumate API manufacturers, exporters, distributors and traders.
click here to find a list of Morniflumate 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 Morniflumate Drug Master File in Korea (Morniflumate KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Morniflumate. The MFDS reviews the Morniflumate KDMF as part of the drug registration process and uses the information provided in the Morniflumate KDMF to evaluate the safety and efficacy of the drug.
After submitting a Morniflumate 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 Morniflumate API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Morniflumate suppliers with KDMF on PharmaCompass.
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