LEBSA- Your strategic API source for niche molecules.
01 1LABORATORIOS ESPINOS Y BOFILL S. A. (LEBSA)
02 1Olon S. p. A.
01 1Chloride dequalinium
02 1Dequalinium chloride
01 1Italy
02 1Spain
LEBSA- Your strategic API source for niche molecules.
Registration Number : 221MF10274
Registrant's Address : Ctra. de l'Hospitalet, 34 08940 Cornella (Barcelona) SPAIN
Initial Date of Registration : 2009-12-15
Latest Date of Registration : 2020-08-05
Registration Number : 219MF10363
Registrant's Address : Strada Rivoltana, km 6/7, 20090 Rodano (MI), Italy
Initial Date of Registration : 2007-12-13
Latest Date of Registration : 2007-12-13
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PharmaCompass offers a list of Dequalinium Chloride 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 Dequalinium Chloride manufacturer or Dequalinium Chloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Dequalinium Chloride manufacturer or Dequalinium Chloride supplier.
PharmaCompass also assists you with knowing the Dequalinium Chloride API Price utilized in the formulation of products. Dequalinium Chloride API Price is not always fixed or binding as the Dequalinium Chloride Price is obtained through a variety of data sources. The Dequalinium Chloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Dekamin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dekamin, including repackagers and relabelers. The FDA regulates Dekamin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dekamin 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 Dekamin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Dekamin supplier is an individual or a company that provides Dekamin active pharmaceutical ingredient (API) or Dekamin finished formulations upon request. The Dekamin suppliers may include Dekamin API manufacturers, exporters, distributors and traders.
click here to find a list of Dekamin 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 Dekamin Drug Master File in Japan (Dekamin JDMF) empowers Dekamin 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 Dekamin JDMF during the approval evaluation for pharmaceutical products. At the time of Dekamin 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 Dekamin suppliers with JDMF on PharmaCompass.
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