Curia - Accelerating therapies from discovery to commercialization with flexible, scalable CDMO solutions.
01 1CURIA SPAIN SAU
02 1Curia Spain SAU
03 2EUROAPI France
04 1Fukuzyu Pharmaceutical Co., Ltd. Toyama Plant_x000D_
05 2Pharmacia & Upjohn Company LLC
06 1Shandong Sirui Pharmaceutical Co., Ltd.
Curia - Accelerating therapies from discovery to commercialization with flexible, scalable CDMO solutions.
Registrant Name : Hwail Pharmaceutical Co., Ltd.
Registration Date : 2022-04-18
Registration Number : 20191203-209-J-494(1)
Manufacturer Name : Curia Spain SAU
Manufacturer Address : Parque Tecnológico Boecillo, Parcela 105, Boecillo, 47151 Valladolid, Spain
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
Registrant Name : AbbVie Korea
Registration Date : 2023-07-03
Registration Number : 20230405-209-J-1469(A)
Manufacturer Name : EUROAPI France
Manufacturer Address : 4 La Paterie, Vertolaye, 63480, France
Curia - Accelerating therapies from discovery to commercialization with flexible, scalable CDMO solutions.
Registrant Name : Sam-O Pharmaceutical Co., Ltd.
Registration Date : 2019-12-03
Registration Number : 20191203-209-J-494
Manufacturer Name : CURIA SPAIN SAU
Manufacturer Address : Parque Tecnologico Parcela 105, Boecillo, 47151 Valladolid, Spain
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
Registrant Name : Novartis Korea
Registration Date : 2023-04-05
Registration Number : 20230405-209-J-1469
Manufacturer Name : EUROAPI France
Manufacturer Address : 4 Lieu Dit La Paterie, Vertolaye, 63480, France
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PharmaCompass offers a list of Dexamethasone 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 Dexamethasone manufacturer or Dexamethasone supplier for your needs.
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A Ozurdex manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ozurdex, including repackagers and relabelers. The FDA regulates Ozurdex manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ozurdex 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 Ozurdex manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Ozurdex supplier is an individual or a company that provides Ozurdex active pharmaceutical ingredient (API) or Ozurdex finished formulations upon request. The Ozurdex suppliers may include Ozurdex API manufacturers, exporters, distributors and traders.
click here to find a list of Ozurdex 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 Ozurdex Drug Master File in Korea (Ozurdex KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Ozurdex. The MFDS reviews the Ozurdex KDMF as part of the drug registration process and uses the information provided in the Ozurdex KDMF to evaluate the safety and efficacy of the drug.
After submitting a Ozurdex 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 Ozurdex API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Ozurdex suppliers with KDMF on PharmaCompass.
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