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
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PharmaCompass offers a list of Aminacrine API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Aminacrine manufacturer or Aminacrine supplier for your needs.
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A Aminacrine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Aminacrine Hydrochloride, including repackagers and relabelers. The FDA regulates Aminacrine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Aminacrine Hydrochloride 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 Hydrochloride supplier is an individual or a company that provides Aminacrine Hydrochloride active pharmaceutical ingredient (API) or Aminacrine Hydrochloride finished formulations upon request. The Aminacrine Hydrochloride suppliers may include Aminacrine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Aminacrine Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 Hydrochloride Drug Master File in Japan (Aminacrine Hydrochloride JDMF) empowers Aminacrine Hydrochloride 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 Hydrochloride JDMF during the approval evaluation for pharmaceutical products. At the time of Aminacrine Hydrochloride 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 Hydrochloride suppliers with JDMF on PharmaCompass.
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