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.
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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 CLARINEX D 24 HOUR manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CLARINEX D 24 HOUR, including repackagers and relabelers. The FDA regulates CLARINEX D 24 HOUR manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CLARINEX D 24 HOUR API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A CLARINEX D 24 HOUR supplier is an individual or a company that provides CLARINEX D 24 HOUR active pharmaceutical ingredient (API) or CLARINEX D 24 HOUR finished formulations upon request. The CLARINEX D 24 HOUR suppliers may include CLARINEX D 24 HOUR API manufacturers, exporters, distributors and traders.
click here to find a list of CLARINEX D 24 HOUR 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 CLARINEX D 24 HOUR Drug Master File in Japan (CLARINEX D 24 HOUR JDMF) empowers CLARINEX D 24 HOUR 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 CLARINEX D 24 HOUR JDMF during the approval evaluation for pharmaceutical products. At the time of CLARINEX D 24 HOUR JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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