01 1Gemini PharmChem Mannheim GmbH
02 2Meiji Seika Pharma Co., Ltd.
03 1MicroBiopharm Japan Co., Ltd.
04 1Olon S. p. A.
05 1Zhejiang Hisun Pharmaceutical Co. , Ltd.
01 1Day stations doxorubicin hydrochloride
02 3Doxorubicin Hydrochloride
03 2Doxorubicin hydrochloride
01 1China
02 1Germany
03 1Italy
04 3Japan
Registration Number : 305MF10028
Registrant's Address : Sandhofer Strasse 96, 68305 Mannheim, Germany
Initial Date of Registration : 2023-02-15
Latest Date of Registration : 2023-02-15
Registration Number : 218MF10960
Registrant's Address : 2-4-16 Kyobashi, Chuo-ku, Tokyo
Initial Date of Registration : 2006-12-01
Latest Date of Registration : 2006-12-01
Registration Number : 302MF10073
Registrant's Address : 2-4-16 Kyobashi, Chuo-ku, Tokyo
Initial Date of Registration : 2020-07-01
Latest Date of Registration : 2020-07-01
Japanese Pharmacopoeia Doxorubicin Hydrochloride
Registration Number : 223MF10126
Registrant's Address : 1-3-1 Kyobashi, Chuo-ku, Tokyo
Initial Date of Registration : 2011-08-09
Latest Date of Registration : 2024-02-21
Registration Number : 303MF10121
Registrant's Address : Strada Rivoltana Km 6/7 20053 Rodano Milano Italy
Initial Date of Registration : 2021-08-02
Latest Date of Registration : 2021-08-02
Registration Number : 226MF10124
Registrant's Address : 46 Waisha Road, Jiaojiang District, Taizhou City, Zhejiang Province, P. R. China 3180...
Initial Date of Registration : 2014-07-01
Latest Date of Registration : 2014-07-01
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PharmaCompass offers a list of Doxorubicin 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 Doxorubicin Hydrochloride manufacturer or Doxorubicin Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Doxorubicin Hydrochloride manufacturer or Doxorubicin Hydrochloride supplier.
PharmaCompass also assists you with knowing the Doxorubicin Hydrochloride API Price utilized in the formulation of products. Doxorubicin Hydrochloride API Price is not always fixed or binding as the Doxorubicin Hydrochloride Price is obtained through a variety of data sources. The Doxorubicin Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Lipodox manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lipodox, including repackagers and relabelers. The FDA regulates Lipodox manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lipodox 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 Lipodox manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Lipodox supplier is an individual or a company that provides Lipodox active pharmaceutical ingredient (API) or Lipodox finished formulations upon request. The Lipodox suppliers may include Lipodox API manufacturers, exporters, distributors and traders.
click here to find a list of Lipodox 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 Lipodox Drug Master File in Japan (Lipodox JDMF) empowers Lipodox 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 Lipodox JDMF during the approval evaluation for pharmaceutical products. At the time of Lipodox 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 Lipodox suppliers with JDMF on PharmaCompass.
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