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01 1Formosa Laboratories, Inc
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01 1Myungmoon Pharmaceutical Co., Ltd.
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01 1Tegapur
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01 1Taiwan
Registrant Name : Myungmoon Pharmaceutical Co., Ltd.
Registration Date : 2021-03-18
Registration Number : 20210318-211-J-894
Manufacturer Name : Formosa Laboratories, Inc
Manufacturer Address : No. 36 & 36-1 Hoping Street, Louchu Country, Taoyuan 33842, Taiwan
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PharmaCompass offers a list of Tegafur 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 Tegafur manufacturer or Tegafur supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Tegafur manufacturer or Tegafur supplier.
PharmaCompass also assists you with knowing the Tegafur API Price utilized in the formulation of products. Tegafur API Price is not always fixed or binding as the Tegafur Price is obtained through a variety of data sources. The Tegafur Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Citofur manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Citofur, including repackagers and relabelers. The FDA regulates Citofur manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Citofur 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 Citofur manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Citofur supplier is an individual or a company that provides Citofur active pharmaceutical ingredient (API) or Citofur finished formulations upon request. The Citofur suppliers may include Citofur API manufacturers, exporters, distributors and traders.
click here to find a list of Citofur suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price 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 Citofur Drug Master File in Korea (Citofur KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Citofur. The MFDS reviews the Citofur KDMF as part of the drug registration process and uses the information provided in the Citofur KDMF to evaluate the safety and efficacy of the drug.
After submitting a Citofur 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 Citofur API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Citofur suppliers with KDMF on PharmaCompass.
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