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 Petimid manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Petimid, including repackagers and relabelers. The FDA regulates Petimid manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Petimid 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 Petimid manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Petimid supplier is an individual or a company that provides Petimid active pharmaceutical ingredient (API) or Petimid finished formulations upon request. The Petimid suppliers may include Petimid API manufacturers, exporters, distributors and traders.
click here to find a list of Petimid 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 Petimid Drug Master File in Japan (Petimid JDMF) empowers Petimid 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 Petimid JDMF during the approval evaluation for pharmaceutical products. At the time of Petimid 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 Petimid suppliers with JDMF on PharmaCompass.
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