01 2Olon S. p. A.
02 1Sicor Societa (') Italiana Corticosteroidi S. r. l.
01 2Daunorubicin Hydrochloride
02 1Daunorubicin hydrochloride
01 3Italy
Registration Number : 305MF10038
Registrant's Address : Strada Rivoltana, km 6/7, 20053 Rodano (MI), Italy
Initial Date of Registration : 2023-03-23
Latest Date of Registration : 2023-03-23
Registration Number : 221MF10078
Registrant's Address : Strada Rivoltana Km 6/7 20090 Rodano Milano Italy
Initial Date of Registration : 2009-04-14
Latest Date of Registration : 2010-02-16
Registration Number : 306MF10068
Registrant's Address : Piazzale Luigi Cadorna, 4 - 20123 MILANO, Italy
Initial Date of Registration : 2024-05-15
Latest Date of Registration : 2024-05-15
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PharmaCompass offers a list of Daunorubicin HCl 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 Daunorubicin HCl manufacturer or Daunorubicin HCl supplier for your needs.
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PharmaCompass also assists you with knowing the Daunorubicin HCl API Price utilized in the formulation of products. Daunorubicin HCl API Price is not always fixed or binding as the Daunorubicin HCl Price is obtained through a variety of data sources. The Daunorubicin HCl Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Cerubidine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cerubidine, including repackagers and relabelers. The FDA regulates Cerubidine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cerubidine 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 Cerubidine supplier is an individual or a company that provides Cerubidine active pharmaceutical ingredient (API) or Cerubidine finished formulations upon request. The Cerubidine suppliers may include Cerubidine API manufacturers, exporters, distributors and traders.
click here to find a list of Cerubidine 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 Cerubidine Drug Master File in Japan (Cerubidine JDMF) empowers Cerubidine 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 Cerubidine JDMF during the approval evaluation for pharmaceutical products. At the time of Cerubidine JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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