01 1CADILA PHARMACEUTICALS LIMITED.
02 1URQUIMA S. A.
01 1Rupatadine fumarate (for manufacturing purposes only)
02 1Rupatajinfumaru salt
01 1India
02 1Spain
Rupatadine fumarate (for manufacturing purposes only)
Registration Number : 306MF10071
Registrant's Address : Sarkhej-Dholka Road, Bhat, Ahmedabad-382 210, Gujarat, INDIA
Initial Date of Registration : 2024-05-29
Latest Date of Registration : 2024-05-29
Registration Number : 228MF10183
Registrant's Address : Poli(´)gon Industrial Riera de Caldes Avinguda Cami(´) Reial 51-57 08184 Palau-Soli...
Initial Date of Registration : 2016-09-09
Latest Date of Registration : 2017-06-30
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PharmaCompass offers a list of Rupatadine Fumarate 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 Rupatadine Fumarate manufacturer or Rupatadine Fumarate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Rupatadine Fumarate manufacturer or Rupatadine Fumarate supplier.
PharmaCompass also assists you with knowing the Rupatadine Fumarate API Price utilized in the formulation of products. Rupatadine Fumarate API Price is not always fixed or binding as the Rupatadine Fumarate Price is obtained through a variety of data sources. The Rupatadine Fumarate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Rupatadin Fumarate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Rupatadin Fumarate, including repackagers and relabelers. The FDA regulates Rupatadin Fumarate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Rupatadin Fumarate 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 Rupatadin Fumarate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Rupatadin Fumarate supplier is an individual or a company that provides Rupatadin Fumarate active pharmaceutical ingredient (API) or Rupatadin Fumarate finished formulations upon request. The Rupatadin Fumarate suppliers may include Rupatadin Fumarate API manufacturers, exporters, distributors and traders.
click here to find a list of Rupatadin Fumarate 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 Rupatadin Fumarate Drug Master File in Japan (Rupatadin Fumarate JDMF) empowers Rupatadin Fumarate 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 Rupatadin Fumarate JDMF during the approval evaluation for pharmaceutical products. At the time of Rupatadin Fumarate 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 Rupatadin Fumarate suppliers with JDMF on PharmaCompass.
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