01 1CADILA PHARMACEUTICALS LIMITED.
02 1Daito Co., Ltd.
03 1Rolabo Outsourcing,S. L.
01 2Desloratadine
02 1Desloratadine (for manufacturing purposes only)
01 1India
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 : 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 Desloratadine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Desloratadine, including repackagers and relabelers. The FDA regulates Desloratadine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Desloratadine 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 Desloratadine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Desloratadine supplier is an individual or a company that provides Desloratadine active pharmaceutical ingredient (API) or Desloratadine finished formulations upon request. The Desloratadine suppliers may include Desloratadine API manufacturers, exporters, distributors and traders.
click here to find a list of Desloratadine 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 Desloratadine Drug Master File in Japan (Desloratadine JDMF) empowers Desloratadine 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 Desloratadine JDMF during the approval evaluation for pharmaceutical products. At the time of Desloratadine 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 Desloratadine suppliers with JDMF on PharmaCompass.
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