01 1Chungking Carelife Pharmaceutical Co., Ltd.
01 1Mitoxantrone Hydrochloride
01 1China
Registration Number : 302MF10131
Registrant's Address : 3 Hua Nanyi Road Chongqing (Changshou) Chemical Industrial Park Chongqing 401254
Initial Date of Registration : 2020-10-26
Latest Date of Registration : 2020-10-26
A Mitoxantrone manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Mitoxantrone, including repackagers and relabelers. The FDA regulates Mitoxantrone manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Mitoxantrone 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 Mitoxantrone manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Mitoxantrone supplier is an individual or a company that provides Mitoxantrone active pharmaceutical ingredient (API) or Mitoxantrone finished formulations upon request. The Mitoxantrone suppliers may include Mitoxantrone API manufacturers, exporters, distributors and traders.
click here to find a list of Mitoxantrone 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 Mitoxantrone Drug Master File in Japan (Mitoxantrone JDMF) empowers Mitoxantrone 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 Mitoxantrone JDMF during the approval evaluation for pharmaceutical products. At the time of Mitoxantrone 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 Mitoxantrone suppliers with JDMF on PharmaCompass.
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