01 1Dongbang FTL Co., Ltd.
01 1Dongbang FTL Co., Ltd.
01 1Mephenamic acid
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, Yakjakgongdan 4-gil, Hyangnam-eup, Hwaseong-si, Gyeonggi-do
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PharmaCompass offers a list of Mefenamic Acid API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Mefenamic Acid manufacturer or Mefenamic Acid supplier for your needs.
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PharmaCompass also assists you with knowing the Mefenamic Acid API Price utilized in the formulation of products. Mefenamic Acid API Price is not always fixed or binding as the Mefenamic Acid Price is obtained through a variety of data sources. The Mefenamic Acid Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Ponstyl Fort manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ponstyl Fort, including repackagers and relabelers. The FDA regulates Ponstyl Fort manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ponstyl Fort 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 Ponstyl Fort supplier is an individual or a company that provides Ponstyl Fort active pharmaceutical ingredient (API) or Ponstyl Fort finished formulations upon request. The Ponstyl Fort suppliers may include Ponstyl Fort 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 Ponstyl Fort Drug Master File in Korea (Ponstyl Fort KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Ponstyl Fort. The MFDS reviews the Ponstyl Fort KDMF as part of the drug registration process and uses the information provided in the Ponstyl Fort KDMF to evaluate the safety and efficacy of the drug.
After submitting a Ponstyl Fort 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 Ponstyl Fort API can apply through the Korea Drug Master File (KDMF).
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