LEBSA- Your strategic API source for niche molecules.
01 2LABORATORIOS ESPINOS Y BOFILL SA (LEBSA)
02 2Ami Lifesciences Private Limited
03 1Olon SPA
LEBSA- Your strategic API source for niche molecules.
Registrant Name : Sam-O Pharmaceutical Co., Ltd.
Registration Date : 2024-11-12
Registration Number : 20220916-211-J-1364(A)
Manufacturer Name : LABORATORIOS ESPINOS Y BOFIL...
Manufacturer Address : Ctra. De L'Hospitalet, 34 08940 Cornellà De Llobregat, Barcelona, Spain
AMI Lifesciences is Driven by Chemistry. Powered by People.
Registrant Name : Medipoem Co., Ltd.
Registration Date : 2025-03-14
Registration Number : 20250205-211-J-1756(1)
Manufacturer Name : Ami Lifesciences Private Lim...
Manufacturer Address : Block No. 82/B, ECP Road At & Post. Karakhadi, Tal-Padra, City : Karakhadi-391450, Di...
LEBSA- Your strategic API source for niche molecules.
Registrant Name : G-Max Pharmachem Co., Ltd.
Registration Date : 2022-09-16
Registration Number : 20220916-211-J-1364
Manufacturer Name : LABORATORIOS ESPINOS Y BOFIL...
Manufacturer Address : Ctra. De L'Hospitalet, 34 08940 Cornellà De Llobregat, Barcelona, Spain
AMI Lifesciences is Driven by Chemistry. Powered by People.
Registrant Name : Aging Life Science Co., Ltd.
Registration Date : 2025-02-05
Registration Number : 20250205-211-J-1756
Manufacturer Name : Ami Lifesciences Private Lim...
Manufacturer Address : Block No. 82/B, ECP Road At & Post. Karakhadi, Tal-Padra, City : Karakhadi-391450, Di...
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PharmaCompass offers a list of Betahistine Dihydrochloride API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Betahistine Dihydrochloride manufacturer or Betahistine Dihydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Betahistine Dihydrochloride manufacturer or Betahistine Dihydrochloride supplier.
A Fidium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fidium, including repackagers and relabelers. The FDA regulates Fidium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fidium 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 Fidium manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Fidium supplier is an individual or a company that provides Fidium active pharmaceutical ingredient (API) or Fidium finished formulations upon request. The Fidium suppliers may include Fidium API manufacturers, exporters, distributors and traders.
click here to find a list of Fidium suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Fidium Drug Master File in Korea (Fidium KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Fidium. The MFDS reviews the Fidium KDMF as part of the drug registration process and uses the information provided in the Fidium KDMF to evaluate the safety and efficacy of the drug.
After submitting a Fidium KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their Fidium API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Fidium suppliers with KDMF on PharmaCompass.
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