01 1Dongbang FTL Co., Ltd.
01 1Dongbang FTL Co., Ltd.
01 1Mepenam Mountain
01 1South Korea
Registrant Name : Dongbang FTL Co., Ltd.
Registration Date : 2019-02-22
Registration Number : 20190222-211-J-312
Manufacturer Name : Dongbang FTL Co., Ltd.
Manufacturer Address : 78, Jeyakgongdan 4-gil, Hyangnam-eup, Hwaseong-si, Gyeonggi-do
82
PharmaCompass offers a list of Mefenamic Acid API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Mefenamic Acid manufacturer or Mefenamic Acid supplier for your needs.
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A Mefanamic acid manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Mefanamic acid, including repackagers and relabelers. The FDA regulates Mefanamic acid manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Mefanamic acid 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 Mefanamic acid manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Mefanamic acid supplier is an individual or a company that provides Mefanamic acid active pharmaceutical ingredient (API) or Mefanamic acid finished formulations upon request. The Mefanamic acid suppliers may include Mefanamic acid API manufacturers, exporters, distributors and traders.
click here to find a list of Mefanamic acid 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 Mefanamic acid Drug Master File in Korea (Mefanamic acid KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Mefanamic acid. The MFDS reviews the Mefanamic acid KDMF as part of the drug registration process and uses the information provided in the Mefanamic acid KDMF to evaluate the safety and efficacy of the drug.
After submitting a Mefanamic acid 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 Mefanamic acid API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Mefanamic acid suppliers with KDMF on PharmaCompass.
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