01 1Zhejiang Apeloa Kangyu Pharmaceutical Co. , Ltd.
01 1Amantadine hydrochloride
01 1China
Registration Number : 223MF10070
Registrant's Address : 333, Jiangnan Road, Hengdian, Dongyang, Zhejiang, 322118, China.
Initial Date of Registration : 2011-05-27
Latest Date of Registration : 2011-05-27
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PharmaCompass also assists you with knowing the Amantadine Hydrochloride API Price utilized in the formulation of products. Amantadine Hydrochloride API Price is not always fixed or binding as the Amantadine Hydrochloride Price is obtained through a variety of data sources. The Amantadine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Amantadine hydrochloride, Symmetrel manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Amantadine hydrochloride, Symmetrel, including repackagers and relabelers. The FDA regulates Amantadine hydrochloride, Symmetrel manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Amantadine hydrochloride, Symmetrel API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Amantadine hydrochloride, Symmetrel supplier is an individual or a company that provides Amantadine hydrochloride, Symmetrel active pharmaceutical ingredient (API) or Amantadine hydrochloride, Symmetrel finished formulations upon request. The Amantadine hydrochloride, Symmetrel suppliers may include Amantadine hydrochloride, Symmetrel API manufacturers, exporters, distributors and traders.
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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 Amantadine hydrochloride, Symmetrel Drug Master File in Japan (Amantadine hydrochloride, Symmetrel JDMF) empowers Amantadine hydrochloride, Symmetrel 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 Amantadine hydrochloride, Symmetrel JDMF during the approval evaluation for pharmaceutical products. At the time of Amantadine hydrochloride, Symmetrel JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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