01 1Liaoyuan Silver Eagle Pharmaceutical Co., Ltd.
01 1Daeshin Pharmaceutical Co., Ltd.
01 1Acrinol hydrate
01 1Blank
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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A Ethacridine Lactate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ethacridine Lactate, including repackagers and relabelers. The FDA regulates Ethacridine Lactate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ethacridine Lactate 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 Ethacridine Lactate supplier is an individual or a company that provides Ethacridine Lactate active pharmaceutical ingredient (API) or Ethacridine Lactate finished formulations upon request. The Ethacridine Lactate suppliers may include Ethacridine Lactate 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 Ethacridine Lactate Drug Master File in Korea (Ethacridine Lactate KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Ethacridine Lactate. The MFDS reviews the Ethacridine Lactate KDMF as part of the drug registration process and uses the information provided in the Ethacridine Lactate KDMF to evaluate the safety and efficacy of the drug.
After submitting a Ethacridine Lactate 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 Ethacridine Lactate API can apply through the Korea Drug Master File (KDMF).
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