01 1Liaoyuan City Yinhawk Anther Co., Ltd.
02 1Liaoyuan Silver Eagle Pharmaceutical Co. , Ltd.
01 2Amino acridine
01 2China
Registration Number : 223MF10153
Registrant's Address : No. 2 Caifu North Road, Friendship Industrial Park, Liaoyuan Economic Development Zon...
Initial Date of Registration : 2011-10-21
Latest Date of Registration : 2011-10-21
Registration Number : 222MF10234
Registrant's Address : No. 100, Lianyang Road, Liaoyuan City, Jilin Province, People's Republic of China
Initial Date of Registration : 2010-09-30
Latest Date of Registration : 2010-09-30
A Aminacrine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Aminacrine, including repackagers and relabelers. The FDA regulates Aminacrine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Aminacrine API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Aminacrine supplier is an individual or a company that provides Aminacrine active pharmaceutical ingredient (API) or Aminacrine finished formulations upon request. The Aminacrine suppliers may include Aminacrine API manufacturers, exporters, distributors and traders.
click here to find a list of Aminacrine 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 Aminacrine Drug Master File in Japan (Aminacrine JDMF) empowers Aminacrine 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 Aminacrine JDMF during the approval evaluation for pharmaceutical products. At the time of Aminacrine 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 Aminacrine suppliers with JDMF on PharmaCompass.
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