01 1Hwail Pharmaceutical Co., Ltd.
01 1Hwail Pharmaceutical Co., Ltd.
01 1Oxatomide
01 1South Korea
Registrant Name : Hwail Pharmaceutical Co., Ltd.
Registration Date : 2005-11-25
Registration Number : 20051125-53-C-210-02
Manufacturer Name : Hwail Pharmaceutical Co., Lt...
Manufacturer Address : 57, Yakjakgongdan 3-gil, Hyangnam-eup, Hwaseong-si, Gyeonggi-do
51
PharmaCompass offers a list of Oxatomide 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 Oxatomide manufacturer or Oxatomide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Oxatomide manufacturer or Oxatomide supplier.
PharmaCompass also assists you with knowing the Oxatomide API Price utilized in the formulation of products. Oxatomide API Price is not always fixed or binding as the Oxatomide Price is obtained through a variety of data sources. The Oxatomide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Oxatomida manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Oxatomida, including repackagers and relabelers. The FDA regulates Oxatomida manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Oxatomida 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 Oxatomida manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Oxatomida supplier is an individual or a company that provides Oxatomida active pharmaceutical ingredient (API) or Oxatomida finished formulations upon request. The Oxatomida suppliers may include Oxatomida API manufacturers, exporters, distributors and traders.
click here to find a list of Oxatomida 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 Oxatomida Drug Master File in Korea (Oxatomida KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Oxatomida. The MFDS reviews the Oxatomida KDMF as part of the drug registration process and uses the information provided in the Oxatomida KDMF to evaluate the safety and efficacy of the drug.
After submitting a Oxatomida 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 Oxatomida API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Oxatomida suppliers with KDMF on PharmaCompass.
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