01 1Chungking CareLife Pharmaceutical Co., Ltd.
01 1Mitoxantrone Hydrochloride
01 1China
Registration Number : 302MF10131
Registrant's Address : 3 Hua Nanyi Road, Chungking Chemical Industrial Park, Chungking 401254
Initial Date of Registration : 2020-10-26
Latest Date of Registration : 2020-10-26
87
PharmaCompass offers a list of Mitoxantrone 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 Mitoxantrone manufacturer or Mitoxantrone supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Mitoxantrone manufacturer or Mitoxantrone supplier.
PharmaCompass also assists you with knowing the Mitoxantrone API Price utilized in the formulation of products. Mitoxantrone API Price is not always fixed or binding as the Mitoxantrone Price is obtained through a variety of data sources. The Mitoxantrone Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A DHAD manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DHAD, including repackagers and relabelers. The FDA regulates DHAD manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DHAD 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 DHAD manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A DHAD supplier is an individual or a company that provides DHAD active pharmaceutical ingredient (API) or DHAD finished formulations upon request. The DHAD suppliers may include DHAD API manufacturers, exporters, distributors and traders.
click here to find a list of DHAD 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 DHAD Drug Master File in Japan (DHAD JDMF) empowers DHAD 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 DHAD JDMF during the approval evaluation for pharmaceutical products. At the time of DHAD 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 DHAD suppliers with JDMF on PharmaCompass.
We have 1 companies offering DHAD
Get in contact with the supplier of your choice:
