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
A Etoposide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Etoposide, including repackagers and relabelers. The FDA regulates Etoposide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Etoposide 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 Etoposide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Etoposide supplier is an individual or a company that provides Etoposide active pharmaceutical ingredient (API) or Etoposide finished formulations upon request. The Etoposide suppliers may include Etoposide API manufacturers, exporters, distributors and traders.
click here to find a list of Etoposide 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 Etoposide Drug Master File in Japan (Etoposide JDMF) empowers Etoposide 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 Etoposide JDMF during the approval evaluation for pharmaceutical products. At the time of Etoposide 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 Etoposide suppliers with JDMF on PharmaCompass.
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