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01 1Liaoyuan Silver Eagle Pharmaceutical Co., Ltd.
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01 1Daeshin Pharmaceutical Co., Ltd.
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01 1Acrinol hydrate
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Registrant Name : Daeshin Pharmaceutical Co., Ltd.
Registration Date : 2025-04-25
Registration Number : 20250425-211-J-1875
Manufacturer Name : Liaoyuan Silver Eagle Pharma...
Manufacturer Address : No.2 Wealth Northern Road, Youyi Industry Area of Liaoyuan Economic Development...
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PharmaCompass offers a list of Ethacridine Lactate 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 Ethacridine Lactate manufacturer or Ethacridine Lactate supplier for your needs.
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PharmaCompass also assists you with knowing the Ethacridine Lactate API Price utilized in the formulation of products. Ethacridine Lactate API Price is not always fixed or binding as the Ethacridine Lactate Price is obtained through a variety of data sources. The Ethacridine Lactate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Ethodin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ethodin, including repackagers and relabelers. The FDA regulates Ethodin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ethodin 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 Ethodin supplier is an individual or a company that provides Ethodin active pharmaceutical ingredient (API) or Ethodin finished formulations upon request. The Ethodin suppliers may include Ethodin 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 Ethodin Drug Master File in Korea (Ethodin KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Ethodin. The MFDS reviews the Ethodin KDMF as part of the drug registration process and uses the information provided in the Ethodin KDMF to evaluate the safety and efficacy of the drug.
After submitting a Ethodin 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 Ethodin API can apply through the Korea Drug Master File (KDMF).
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