01 1CARBOGEN AMCIS AG
01 1Nepafenac
01 1Switzerland
Registration Number : 222MF10160
Registrant's Address : Hauptstrasse 171, CH-4416 Bubendorf, Switzerland
Initial Date of Registration : 2010-05-31
Latest Date of Registration : 2010-05-31
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PharmaCompass offers a list of Nepafenac 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 Nepafenac manufacturer or Nepafenac supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Nepafenac manufacturer or Nepafenac supplier.
PharmaCompass also assists you with knowing the Nepafenac API Price utilized in the formulation of products. Nepafenac API Price is not always fixed or binding as the Nepafenac Price is obtained through a variety of data sources. The Nepafenac Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A ILEVRO manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of ILEVRO, including repackagers and relabelers. The FDA regulates ILEVRO manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. ILEVRO 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 ILEVRO manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A ILEVRO supplier is an individual or a company that provides ILEVRO active pharmaceutical ingredient (API) or ILEVRO finished formulations upon request. The ILEVRO suppliers may include ILEVRO API manufacturers, exporters, distributors and traders.
click here to find a list of ILEVRO 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 ILEVRO Drug Master File in Japan (ILEVRO JDMF) empowers ILEVRO 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 ILEVRO JDMF during the approval evaluation for pharmaceutical products. At the time of ILEVRO 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 ILEVRO suppliers with JDMF on PharmaCompass.
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