01 1Gemini PharmChem Mannheim GmbH
02 1Japan Microbiopharmacist Co., Ltd.
03 2Meiji Seika Pharma 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, and more, enabling you to easily find the right Doxorubicin Hydrochloride manufacturer or Doxorubicin Hydrochloride supplier for your needs.
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A Doxorubicin HCl manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Doxorubicin HCl, including repackagers and relabelers. The FDA regulates Doxorubicin HCl manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Doxorubicin HCl API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Doxorubicin HCl supplier is an individual or a company that provides Doxorubicin HCl active pharmaceutical ingredient (API) or Doxorubicin HCl finished formulations upon request. The Doxorubicin HCl suppliers may include Doxorubicin HCl API manufacturers, exporters, distributors and traders.
click here to find a list of Doxorubicin HCl suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 Doxorubicin HCl Drug Master File in Japan (Doxorubicin HCl JDMF) empowers Doxorubicin HCl 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 Doxorubicin HCl JDMF during the approval evaluation for pharmaceutical products. At the time of Doxorubicin HCl 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 Doxorubicin HCl suppliers with JDMF on PharmaCompass.
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