01 1Katwijk Chemie BV
01 1Lee Sung International Co., Ltd.
01 1Ethosuximide
01 1Netherlands
Registrant Name : Lee Sung International Co., Ltd.
Registration Date : 2022-11-24
Registration Number : 20221124-211-J-1411
Manufacturer Name : Katwijk Chemie BV
Manufacturer Address : Snijdersteaat 6, Katwijk Zh, 2222 BA, Netherlands
100
PharmaCompass offers a list of Ethosuximide 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 Ethosuximide manufacturer or Ethosuximide supplier for your needs.
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PharmaCompass also assists you with knowing the Ethosuximide API Price utilized in the formulation of products. Ethosuximide API Price is not always fixed or binding as the Ethosuximide Price is obtained through a variety of data sources. The Ethosuximide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Etomal manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Etomal, including repackagers and relabelers. The FDA regulates Etomal manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Etomal 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 Etomal supplier is an individual or a company that provides Etomal active pharmaceutical ingredient (API) or Etomal finished formulations upon request. The Etomal suppliers may include Etomal API manufacturers, exporters, distributors and traders.
click here to find a list of Etomal 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 Etomal Drug Master File in Korea (Etomal KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Etomal. The MFDS reviews the Etomal KDMF as part of the drug registration process and uses the information provided in the Etomal KDMF to evaluate the safety and efficacy of the drug.
After submitting a Etomal 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 Etomal API can apply through the Korea Drug Master File (KDMF).
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