Evonik's CDMO solutions for APIs and HPAPIs: It specializes where the client needs it most!
01 1Evonik Operations GmbH
02 1Esteve Huayi Pharmaceutical Co., Ltd.
03 1Laurus Labs Limited(Unit-3)
04 1Union Quimico Farmaceutica S.A. (Uquifa)
05 1Yuhan Chemical Co., Ltd.
01 1Aging Life Science Co., Ltd.
02 4Gilead Sciences Korea Ltd.
01 5Emtricitabine
01 1China
02 1Germany
03 1India
04 1South Korea
05 1Spain
Evonik's CDMO solutions for APIs and HPAPIs: It specializes where the client needs it most!
Registrant Name : Gilead Sciences Korea Ltd.
Registration Date : 2014-12-04
Registration Number : No. 4945-20-ND
Manufacturer Name : Evonik Operations GmbH
Manufacturer Address : Gutenbergstrasse 2, 69221 Dossenheim, Germany
Registrant Name : Gilead Sciences Korea Ltd.
Registration Date : 2021-02-25
Registration Number : 205-21-ND
Manufacturer Name : Esteve Huayi Pharmaceutical ...
Manufacturer Address : Linhai Road, Yuecheng District, Shaoxing, 312071 Zhejiang China
Registrant Name : Aging Life Science Co., Ltd.
Registration Date : 2020-07-15
Registration Number : Su434-17-ND
Manufacturer Name : Laurus Labs Limited(Unit-3)
Manufacturer Address : Plot No. 18, Jawaharlal Nehru Pharma City, Parawada, Visakhapatnam - 531 021, Andhra ...
Registrant Name : Gilead Sciences Korea Ltd.
Registration Date : 2017-05-16
Registration Number : Su205-13-ND
Manufacturer Name : Union Quimico Farmaceutica S...
Manufacturer Address : Poligono Industrial Moli de les Planes, Calle Font de Bocs S/N, C35 KM 57 08470 Sant ...
Registrant Name : Gilead Sciences Korea Ltd.
Registration Date : 2014-05-30
Registration Number : 1646-18-ND
Manufacturer Name : Yuhan Chemical Co., Ltd.
Manufacturer Address : 45 Jiwon-ro, Danwon-gu, Ansan-si, Gyeonggi-do
A Emtriva manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Emtriva, including repackagers and relabelers. The FDA regulates Emtriva manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Emtriva 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 Emtriva manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Emtriva supplier is an individual or a company that provides Emtriva active pharmaceutical ingredient (API) or Emtriva finished formulations upon request. The Emtriva suppliers may include Emtriva API manufacturers, exporters, distributors and traders.
click here to find a list of Emtriva 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 Emtriva Drug Master File in Korea (Emtriva KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Emtriva. The MFDS reviews the Emtriva KDMF as part of the drug registration process and uses the information provided in the Emtriva KDMF to evaluate the safety and efficacy of the drug.
After submitting a Emtriva 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 Emtriva API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Emtriva suppliers with KDMF on PharmaCompass.
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