01 1CADILA PHARMACEUTICALS LIMITED.
02 1Daito Co., Ltd.
03 1Hetero Labs Limited
04 1Rolabo Outsourcing,S. L.
01 2Desloratadine
02 1Desloratadine
03 1Desloratadine (for manufacturing purposes only)
01 2India
02 1Japan
03 1Spain
Desloratadine (for manufacturing purposes only)
Registration Number : 307MF10040
Registrant's Address : Sarkhej-Dholka Road, Bhat, Ahmedabad-382 210, Gujarat, INDIA
Initial Date of Registration : 2025-02-26
Latest Date of Registration : 2025-02-26
Registration Number : 307MF10009
Registrant's Address : 326 Yokamachi, Toyama City, Toyama Prefecture
Initial Date of Registration : 2025-01-09
Latest Date of Registration : 2025-01-09
Registration Number : 307MF10142
Registrant's Address : 7-2-A2, Industrial Estates, Sanath Nagar, Hyderabad-500 018, Telangana, INDIA
Initial Date of Registration : 2025-11-26
Latest Date of Registration : 2025-11-26
Registration Number : 307MF10031
Registrant's Address : Poligono Industrial Malpica C/J, No. :3-4 50016 Zaragoza, Spain
Initial Date of Registration : 2025-02-07
Latest Date of Registration : 2025-02-07
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PharmaCompass offers a list of Desloratadine 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 Desloratadine manufacturer or Desloratadine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Desloratadine manufacturer or Desloratadine supplier.
PharmaCompass also assists you with knowing the Desloratadine API Price utilized in the formulation of products. Desloratadine API Price is not always fixed or binding as the Desloratadine Price is obtained through a variety of data sources. The Desloratadine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Opulis manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Opulis, including repackagers and relabelers. The FDA regulates Opulis manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Opulis 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 Opulis manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Opulis supplier is an individual or a company that provides Opulis active pharmaceutical ingredient (API) or Opulis finished formulations upon request. The Opulis suppliers may include Opulis API manufacturers, exporters, distributors and traders.
click here to find a list of Opulis 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 Opulis Drug Master File in Japan (Opulis JDMF) empowers Opulis 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 Opulis JDMF during the approval evaluation for pharmaceutical products. At the time of Opulis 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 Opulis suppliers with JDMF on PharmaCompass.
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