01 1Hana Pharmaceutical Co., Ltd.
01 1Hana Pharmaceutical Co., Ltd.
01 1Flacainide acetate
01 1South Korea
Registrant Name : Hana Pharmaceutical Co., Ltd.
Registration Date : 2021-03-23
Registration Number : 20210323-211-J-896
Manufacturer Name : Hana Pharmaceutical Co., Ltd...
Manufacturer Address : 133, Jeyakgongdan 3-gil, Hyangnam-eup, Hwaseong-si, Gyeonggi-do
48
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A Flecainide Acetate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Flecainide Acetate, including repackagers and relabelers. The FDA regulates Flecainide Acetate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Flecainide Acetate 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 Flecainide Acetate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Flecainide Acetate supplier is an individual or a company that provides Flecainide Acetate active pharmaceutical ingredient (API) or Flecainide Acetate finished formulations upon request. The Flecainide Acetate suppliers may include Flecainide Acetate API manufacturers, exporters, distributors and traders.
click here to find a list of Flecainide Acetate suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 Flecainide Acetate Drug Master File in Korea (Flecainide Acetate KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Flecainide Acetate. The MFDS reviews the Flecainide Acetate KDMF as part of the drug registration process and uses the information provided in the Flecainide Acetate KDMF to evaluate the safety and efficacy of the drug.
After submitting a Flecainide Acetate 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 Flecainide Acetate API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Flecainide Acetate suppliers with KDMF on PharmaCompass.
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