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01 1Zhejiang Hisun Pharmaceutical. Co., Ltd.
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01 1Korea United Pharmaceutical Co., Ltd.
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01 1Dactinomycin
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01 1China
Registrant Name : Korea United Pharmaceutical Co., Ltd.
Registration Date : 2020-07-14
Registration Number : 20200714-210-J-490
Manufacturer Name : Zhejiang Hisun Pharmaceutica...
Manufacturer Address : No. 56 Binhai Road, Jiaojiang District, Taizhou City, Zhejiang China
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PharmaCompass offers a list of Dactinomycin 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 Dactinomycin manufacturer or Dactinomycin supplier for your needs.
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PharmaCompass also assists you with knowing the Dactinomycin API Price utilized in the formulation of products. Dactinomycin API Price is not always fixed or binding as the Dactinomycin Price is obtained through a variety of data sources. The Dactinomycin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Lyovac cosmegen manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lyovac cosmegen, including repackagers and relabelers. The FDA regulates Lyovac cosmegen manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lyovac cosmegen 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 Lyovac cosmegen supplier is an individual or a company that provides Lyovac cosmegen active pharmaceutical ingredient (API) or Lyovac cosmegen finished formulations upon request. The Lyovac cosmegen suppliers may include Lyovac cosmegen 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 Lyovac cosmegen Drug Master File in Korea (Lyovac cosmegen KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Lyovac cosmegen. The MFDS reviews the Lyovac cosmegen KDMF as part of the drug registration process and uses the information provided in the Lyovac cosmegen KDMF to evaluate the safety and efficacy of the drug.
After submitting a Lyovac cosmegen 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 Lyovac cosmegen API can apply through the Korea Drug Master File (KDMF).
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