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