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, Price,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.
PharmaCompass also assists you with knowing the Etoposide API Price utilized in the formulation of products. Etoposide API Price is not always fixed or binding as the Etoposide Price is obtained through a variety of data sources. The Etoposide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A EPEG manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of EPEG, including repackagers and relabelers. The FDA regulates EPEG manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. EPEG 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 EPEG manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A EPEG supplier is an individual or a company that provides EPEG active pharmaceutical ingredient (API) or EPEG finished formulations upon request. The EPEG suppliers may include EPEG API manufacturers, exporters, distributors and traders.
click here to find a list of EPEG 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 EPEG Drug Master File in Japan (EPEG JDMF) empowers EPEG 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 EPEG JDMF during the approval evaluation for pharmaceutical products. At the time of EPEG 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 EPEG suppliers with JDMF on PharmaCompass.
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