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
A Dequalinium Chloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dequalinium Chloride, including repackagers and relabelers. The FDA regulates Dequalinium Chloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dequalinium Chloride 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 Dequalinium Chloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Dequalinium Chloride supplier is an individual or a company that provides Dequalinium Chloride active pharmaceutical ingredient (API) or Dequalinium Chloride finished formulations upon request. The Dequalinium Chloride suppliers may include Dequalinium Chloride API manufacturers, exporters, distributors and traders.
click here to find a list of Dequalinium Chloride 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 Dequalinium Chloride Drug Master File in Japan (Dequalinium Chloride JDMF) empowers Dequalinium Chloride 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 Dequalinium Chloride JDMF during the approval evaluation for pharmaceutical products. At the time of Dequalinium Chloride 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 Dequalinium Chloride suppliers with JDMF on PharmaCompass.
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