01 1Cipla Limited
02 1Sicor Societa (') Italiana Corticosteroidi S. r. l.
01 1Etoposide
02 1Etoposide "Teva"
01 1India
02 1Italy
Registration Number : 222MF10214
Registrant's Address : Cipla House, Peninsula Business Park, Ganpatrao Kadam Marg, Lower Parel, Mumbai - 400...
Initial Date of Registration : 2010-08-05
Latest Date of Registration : 2010-08-05
Registration Number : 218MF10457
Registrant's Address : Piazzale Luigi Cadorna, 4-20123 MILANO, Italy
Initial Date of Registration : 2006-04-27
Latest Date of Registration : 2021-08-19
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PharmaCompass offers a list of Etoposide 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 Etoposide manufacturer or Etoposide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Etoposide manufacturer or Etoposide supplier.
A Etopol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Etopol, including repackagers and relabelers. The FDA regulates Etopol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Etopol 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 Etopol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Etopol supplier is an individual or a company that provides Etopol active pharmaceutical ingredient (API) or Etopol finished formulations upon request. The Etopol suppliers may include Etopol API manufacturers, exporters, distributors and traders.
click here to find a list of Etopol 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 Etopol Drug Master File in Japan (Etopol JDMF) empowers Etopol 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 Etopol JDMF during the approval evaluation for pharmaceutical products. At the time of Etopol 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 Etopol suppliers with JDMF on PharmaCompass.
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