Centrient is a leading manufacturer of Beta-Lactam Antibiotics and a provider of next-generation Statins and Antifungals.
01 3Centrient Pharmaceuticals Spain S.A.
02 9ACS DOBFAR SpA
03 1Aurobindo Pharma Limited (Unit-XI)
04 4Lupin Limited
05 2Orchid Pharma Limited
Centrient is a leading manufacturer of Beta-Lactam Antibiotics and a provider of next-generation Statins and Antifungals.
Registrant Name : Daewoong Bio Co., Ltd.
Registration Date : 2019-04-04
Registration Number : 20050831-19-A-15-05(3)
Manufacturer Name : Centrient Pharmaceuticals Sp...
Manufacturer Address : C/Ripolles, n2 Poligono Industrial URVASA Santa Perpetua de Mogoda 08130 BARCELONA SP...
Centrient is a leading manufacturer of Beta-Lactam Antibiotics and a provider of next-generation Statins and Antifungals.
Registrant Name : Daewoong Pharmaceutical Co., Ltd.
Registration Date : 2015-05-12
Registration Number : 20050831-19-A-15-05(2)
Manufacturer Name : Centrient Pharmaceuticals Sp...
Manufacturer Address : C/Ripolles, n2 Poligono Industrial URVASA Santa Perpetua de Mogoda 08130 BARCELONA SP...
Centrient is a leading manufacturer of Beta-Lactam Antibiotics and a provider of next-generation Statins and Antifungals.
Registrant Name : Aging Life Science Co., Ltd.
Registration Date : 2005-08-31
Registration Number : 20050831-19-A-15-05
Manufacturer Name : Centrient Pharmaceuticals Sp...
Manufacturer Address : C/Ripolles, n2 Poligono Industrial URVASA Santa Perpetua de Mogoda 08130 BARCELONA SP...
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A CEFADROXIL/CEFADROXIL HEMIHYDRATE manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CEFADROXIL/CEFADROXIL HEMIHYDRATE, including repackagers and relabelers. The FDA regulates CEFADROXIL/CEFADROXIL HEMIHYDRATE manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CEFADROXIL/CEFADROXIL HEMIHYDRATE 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 CEFADROXIL/CEFADROXIL HEMIHYDRATE supplier is an individual or a company that provides CEFADROXIL/CEFADROXIL HEMIHYDRATE active pharmaceutical ingredient (API) or CEFADROXIL/CEFADROXIL HEMIHYDRATE finished formulations upon request. The CEFADROXIL/CEFADROXIL HEMIHYDRATE suppliers may include CEFADROXIL/CEFADROXIL HEMIHYDRATE API manufacturers, exporters, distributors and traders.
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In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a CEFADROXIL/CEFADROXIL HEMIHYDRATE Drug Master File in Korea (CEFADROXIL/CEFADROXIL HEMIHYDRATE KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of CEFADROXIL/CEFADROXIL HEMIHYDRATE. The MFDS reviews the CEFADROXIL/CEFADROXIL HEMIHYDRATE KDMF as part of the drug registration process and uses the information provided in the CEFADROXIL/CEFADROXIL HEMIHYDRATE KDMF to evaluate the safety and efficacy of the drug.
After submitting a CEFADROXIL/CEFADROXIL HEMIHYDRATE 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 CEFADROXIL/CEFADROXIL HEMIHYDRATE API can apply through the Korea Drug Master File (KDMF).
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