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