01 1Gemini PharmChem Mannheim GmbH
02 1MicroBiopharm Japan Co., Ltd.
03 1Olon S. p. A.
04 1Sicor Societa (') Italiana Corticosteroidi S. r. l.
05 1Synbias Pharma. Ltd.
01 1Day stations epirubicin hydrochloride
02 2Epirubicin Hydrochloride
03 1Epirubicin hydrochloride
04 1Epirubicin hydrochloride "Teva"
01 1Germany
02 2Italy
03 1Japan
04 1Ukraine
Registration Number : 303MF10147
Registrant's Address : Sandhofer Strasse 96, 68305 Mannheim, Germany
Initial Date of Registration : 2021-09-09
Latest Date of Registration : 2023-02-02
Registration Number : 223MF10127
Registrant's Address : 1-3-1 Kyobashi, Chuo-ku, Tokyo
Initial Date of Registration : 2011-08-09
Latest Date of Registration : 2022-11-16
Registration Number : 301MF10102
Registrant's Address : Strada Rivoltana Km 6/7 20090 Rodano Milano Italy
Initial Date of Registration : 2019-12-03
Latest Date of Registration : 2019-12-03
Epirubicin Hydrochloride "Teva"
Registration Number : 218MF10879
Registrant's Address : Piazzale Luigi Cadorna, 4-20123 MILANO, Italy
Initial Date of Registration : 2006-11-10
Latest Date of Registration : 2006-11-10
Registration Number : 222MF10019
Registrant's Address : Georgievskaya Str. 30a, 87515 Mariupol, Ukraine
Initial Date of Registration : 2010-01-14
Latest Date of Registration : 2010-01-14
22
PharmaCompass offers a list of Epirubicin 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 Epirubicin Hydrochloride manufacturer or Epirubicin Hydrochloride supplier for your needs.
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PharmaCompass also assists you with knowing the Epirubicin Hydrochloride API Price utilized in the formulation of products. Epirubicin Hydrochloride API Price is not always fixed or binding as the Epirubicin Hydrochloride Price is obtained through a variety of data sources. The Epirubicin Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Epilem manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Epilem, including repackagers and relabelers. The FDA regulates Epilem manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Epilem 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 Epilem manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Epilem supplier is an individual or a company that provides Epilem active pharmaceutical ingredient (API) or Epilem finished formulations upon request. The Epilem suppliers may include Epilem API manufacturers, exporters, distributors and traders.
click here to find a list of Epilem 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 Epilem Drug Master File in Japan (Epilem JDMF) empowers Epilem 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 Epilem JDMF during the approval evaluation for pharmaceutical products. At the time of Epilem 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 Epilem suppliers with JDMF on PharmaCompass.
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