01 1CHEMI S. p. A.
02 1DIVI'S LABORATORIES LIMITED
01 2Nabumetone
01 1India
02 1Italy
Registration Number : 224MF10109
Registrant's Address : Viale dei Laboratori 54, 20092 Cinisello Balsamo (Milano), Italy
Initial Date of Registration : 2012-06-22
Latest Date of Registration : 2012-06-22
Registration Number : 228MF10204
Registrant's Address : 1-72/23(P)/DIVIS/303, Divi Towers Cyber Hills, Gachibowli Hyderabad - 500 032 T...
Initial Date of Registration : 2016-10-31
Latest Date of Registration : 2016-10-31
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PharmaCompass offers a list of Nabumetone 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 Nabumetone manufacturer or Nabumetone supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Nabumetone manufacturer or Nabumetone supplier.
PharmaCompass also assists you with knowing the Nabumetone API Price utilized in the formulation of products. Nabumetone API Price is not always fixed or binding as the Nabumetone Price is obtained through a variety of data sources. The Nabumetone Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Relifen manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Relifen, including repackagers and relabelers. The FDA regulates Relifen manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Relifen 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 Relifen manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Relifen supplier is an individual or a company that provides Relifen active pharmaceutical ingredient (API) or Relifen finished formulations upon request. The Relifen suppliers may include Relifen API manufacturers, exporters, distributors and traders.
click here to find a list of Relifen 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 Relifen Drug Master File in Japan (Relifen JDMF) empowers Relifen 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 Relifen JDMF during the approval evaluation for pharmaceutical products. At the time of Relifen 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 Relifen suppliers with JDMF on PharmaCompass.
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