Farmak works in the development, production and marketing of APIs, Intermediates & Specialties// FDA inspected.
01 1Farmak, as
02 1EUROAPI FRANCE
03 1Sanofi Chimie
04 1Glenmark Life Sciences Limited
05 1ScinoPharm Taiwan, Ltd.
Farmak works in the development, production and marketing of APIs, Intermediates & Specialties// FDA inspected.
Registrant Name : Kukjeon Pharmaceutical Co., Ltd.
Registration Date : 2013-12-19
Registration Number : No. 4749-12-ND
Manufacturer Name : Farmak, as
Manufacturer Address : Na vlcinci 16/3, Klasterni Hradisko, 779 00 Olomouc, Czech Republic
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
Registrant Name : Sanofi-Aventis Korea Co., Ltd.
Registration Date : 2012-08-31
Registration Number : 3025-5-ND
Manufacturer Name : EUROAPI FRANCE
Manufacturer Address : 4 La Paterie, 63480, Vertolaye, France
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
Registrant Name : Sanofi-Aventis Korea Co., Ltd.
Registration Date : 2008-05-07
Registration Number : 3025-2-ND
Manufacturer Name : Sanofi Chimie
Manufacturer Address : Center de production de Vitry-sur-Seine9, Quai Jules Guesde 94403 Vitry SUR Seine Ced...
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PharmaCompass offers a list of Riluzole 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 Riluzole manufacturer or Riluzole supplier for your needs.
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A NCGC00015882-12 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of NCGC00015882-12, including repackagers and relabelers. The FDA regulates NCGC00015882-12 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. NCGC00015882-12 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 NCGC00015882-12 supplier is an individual or a company that provides NCGC00015882-12 active pharmaceutical ingredient (API) or NCGC00015882-12 finished formulations upon request. The NCGC00015882-12 suppliers may include NCGC00015882-12 API manufacturers, exporters, distributors and traders.
click here to find a list of NCGC00015882-12 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price 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 NCGC00015882-12 Drug Master File in Korea (NCGC00015882-12 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of NCGC00015882-12. The MFDS reviews the NCGC00015882-12 KDMF as part of the drug registration process and uses the information provided in the NCGC00015882-12 KDMF to evaluate the safety and efficacy of the drug.
After submitting a NCGC00015882-12 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 NCGC00015882-12 API can apply through the Korea Drug Master File (KDMF).
click here to find a list of NCGC00015882-12 suppliers with KDMF on PharmaCompass.
We have 4 companies offering NCGC00015882-12
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