01 1Zhejiang Hisoar Chuannan Pharmaceutical Co. , Ltd.
01 1Clindamycin hydrochlide monohydrate
01 1China
Clindamycin hydrochloride monohydrate
Registration Number : 303MF10077
Registrant's Address : No. 23,5th Donghai Avenue Zhejiang Chemical materials base Linhai zone, Linhai City, ...
Initial Date of Registration : 2021-05-13
Latest Date of Registration : 2021-05-13
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PharmaCompass offers a list of Clindamycin Hydrochloride 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 Clindamycin Hydrochloride manufacturer or Clindamycin Hydrochloride supplier for your needs.
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PharmaCompass also assists you with knowing the Clindamycin Hydrochloride API Price utilized in the formulation of products. Clindamycin Hydrochloride API Price is not always fixed or binding as the Clindamycin Hydrochloride Price is obtained through a variety of data sources. The Clindamycin Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Acanya manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Acanya, including repackagers and relabelers. The FDA regulates Acanya manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Acanya 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 Acanya supplier is an individual or a company that provides Acanya active pharmaceutical ingredient (API) or Acanya finished formulations upon request. The Acanya suppliers may include Acanya API manufacturers, exporters, distributors and traders.
click here to find a list of Acanya 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 Acanya Drug Master File in Japan (Acanya JDMF) empowers Acanya 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 Acanya JDMF during the approval evaluation for pharmaceutical products. At the time of Acanya 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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