Interquim comes from an international group of 50 companies active in the pharma, hospital, diagnostics, fine chemicals & feed sectors.
01 1Interquim, SA
02 1MSN Laboratories PVT.LTD
03 1MSN Laboratories Private Limited
04 1Takeda GmbH, Production site Singen
01 1AstraZeneca Korea
02 2Pharmapia Co., Ltd.
03 1Seongyi Bio Co., Ltd.
01 3Loflumilast
02 1Undifferentiated flumilast
01 2India
02 1Japan
03 1Spain
Interquim comes from an international group of 50 companies active in the pharma, hospital, diagnostics, fine chemicals & feed sectors.
Registrant Name : Seongyi Bio Co., Ltd.
Registration Date : 2016-12-29
Registration Number : Su259-4-ND
Manufacturer Name : Interquim, SA
Manufacturer Address : Joan Buscalla 10, E-08173 Sant Cugat del Valles, Barcelona, Spain
Registrant Name : Pharmapia Co., Ltd.
Registration Date : 2021-07-20
Registration Number : Su258-14-ND
Manufacturer Name : MSN Laboratories PVT.LTD
Manufacturer Address : Sy. No. 317 , 320, 321, 322, 323, 604 & 605, Rudraram (Village), Patancheru (Mandal),...
Registrant Name : Pharmapia Co., Ltd.
Registration Date : 2017-04-03
Registration Number : Su258-2-ND
Manufacturer Name : MSN Laboratories Private Lim...
Manufacturer Address : Sy. No. 317, 320, 321, 322, 323, 604 & 605, Rudraram (Village), Patancheru (Mandal), ...
Registrant Name : AstraZeneca Korea
Registration Date : 2011-04-29
Registration Number : Su5550-1-ND
Manufacturer Name : Takeda GmbH, Production site...
Manufacturer Address : Robert-Bosch-Strass 8 78224 Singen Germany
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PharmaCompass offers a list of Roflumilast 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 Roflumilast manufacturer or Roflumilast supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Roflumilast manufacturer or Roflumilast supplier.
A Libertek manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Libertek, including repackagers and relabelers. The FDA regulates Libertek manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Libertek 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 Libertek manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Libertek supplier is an individual or a company that provides Libertek active pharmaceutical ingredient (API) or Libertek finished formulations upon request. The Libertek suppliers may include Libertek API manufacturers, exporters, distributors and traders.
click here to find a list of Libertek 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 Libertek Drug Master File in Korea (Libertek KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Libertek. The MFDS reviews the Libertek KDMF as part of the drug registration process and uses the information provided in the Libertek KDMF to evaluate the safety and efficacy of the drug.
After submitting a Libertek 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 Libertek API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Libertek suppliers with KDMF on PharmaCompass.
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