01 1Sicor Societa (') Italiana Corticosteroidi S. r. l.
01 1Dexrazoxane "Teva"
01 1Italy
Registration Number : 224MF10205
Registrant's Address : Piazzale Luigi Cadorna, 4 - 20123 MILANO, Italy
Initial Date of Registration : 2012-10-09
Latest Date of Registration : 2021-01-20
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PharmaCompass offers a list of Dexrazoxane 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 Dexrazoxane manufacturer or Dexrazoxane supplier for your needs.
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PharmaCompass also assists you with knowing the Dexrazoxane API Price utilized in the formulation of products. Dexrazoxane API Price is not always fixed or binding as the Dexrazoxane Price is obtained through a variety of data sources. The Dexrazoxane Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Dexrazoxane HCl manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dexrazoxane HCl, including repackagers and relabelers. The FDA regulates Dexrazoxane HCl manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dexrazoxane 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 Dexrazoxane HCl supplier is an individual or a company that provides Dexrazoxane HCl active pharmaceutical ingredient (API) or Dexrazoxane HCl finished formulations upon request. The Dexrazoxane HCl suppliers may include Dexrazoxane HCl API manufacturers, exporters, distributors and traders.
click here to find a list of Dexrazoxane HCl 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 Dexrazoxane HCl Drug Master File in Japan (Dexrazoxane HCl JDMF) empowers Dexrazoxane 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 Dexrazoxane HCl JDMF during the approval evaluation for pharmaceutical products. At the time of Dexrazoxane HCl 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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