01 1Katwijk Chemie bv
01 1Ethosuximide
01 1Netherlands
Registration Number : 217MF10735
Registrant's Address : Snijderstraat 6,2222 BA, Katwijk, ZH The Netherlands
Initial Date of Registration : 2005-10-07
Latest Date of Registration : 2024-11-20
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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.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ethosuximide manufacturer or Ethosuximide supplier.
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 Petnidan manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Petnidan, including repackagers and relabelers. The FDA regulates Petnidan manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Petnidan 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 Petnidan manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Petnidan supplier is an individual or a company that provides Petnidan active pharmaceutical ingredient (API) or Petnidan finished formulations upon request. The Petnidan suppliers may include Petnidan API manufacturers, exporters, distributors and traders.
click here to find a list of Petnidan suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Petnidan Drug Master File in Japan (Petnidan JDMF) empowers Petnidan API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Petnidan JDMF during the approval evaluation for pharmaceutical products. At the time of Petnidan JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Petnidan suppliers with JDMF on PharmaCompass.
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