01 1Liaoning Beiqi Pharmaceutical Co. , Ltd.
01 1Ethionamide
01 1China
Registration Number : 221MF10259
Registrant's Address : No. 18-6, Huanghai Street, Zhenxing District, Dandong City, China
Initial Date of Registration : 2009-12-03
Latest Date of Registration : 2009-12-03
A Ethionamide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ethionamide, including repackagers and relabelers. The FDA regulates Ethionamide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ethionamide 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 Ethionamide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ethionamide supplier is an individual or a company that provides Ethionamide active pharmaceutical ingredient (API) or Ethionamide finished formulations upon request. The Ethionamide suppliers may include Ethionamide API manufacturers, exporters, distributors and traders.
click here to find a list of Ethionamide 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 Ethionamide Drug Master File in Japan (Ethionamide JDMF) empowers Ethionamide 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 Ethionamide JDMF during the approval evaluation for pharmaceutical products. At the time of Ethionamide 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 Ethionamide suppliers with JDMF on PharmaCompass.
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