01 1AbbVie Inc.
02 3CONCORD BIOTECH LIMITED
03 1Chong Kun Dang Bio Co., Ltd. @ Chong Kun Dang Bio Co., Ltd.
04 1Chong Kun Dang Bio Co., Ltd._x000D_
05 1Curia Italy Srl
06 1Joyang Laboratories
07 1Sicor Societa' Italiana Corticosteroidi SRL
08 1Sterling Pharma Ringaskiddy Limited@[Suanfarma Manufacturer] Sandoz GmbH_x000D_ @Suanfarma Italia SpA
09 1Teva Czech Industries sro@Teva Pharmaceutical Works Private Limited Company@Teva Pharmaceutical Works Private Limited Company
10 1Teva Czech Industries sro@[Grade Manufacturer] Teva Pharmaceutical Works Private Limited Company@[Grade Manufacturer] Teva Pharmaceutical Works Private Limited Company
Registrant Name : AbbVie Korea Inc.
Registration Date : 2005-08-31
Registration Number : 20050831-18-C-100-05
Manufacturer Name : AbbVie Inc.
Manufacturer Address : 1401 Sheridan Road, North Chicago, IL, 60064-4000, USA
A Cyclosporine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cyclosporine, including repackagers and relabelers. The FDA regulates Cyclosporine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cyclosporine 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 Cyclosporine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cyclosporine supplier is an individual or a company that provides Cyclosporine active pharmaceutical ingredient (API) or Cyclosporine finished formulations upon request. The Cyclosporine suppliers may include Cyclosporine API manufacturers, exporters, distributors and traders.
click here to find a list of Cyclosporine 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 Cyclosporine Drug Master File in Korea (Cyclosporine KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Cyclosporine. The MFDS reviews the Cyclosporine KDMF as part of the drug registration process and uses the information provided in the Cyclosporine KDMF to evaluate the safety and efficacy of the drug.
After submitting a Cyclosporine 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 Cyclosporine API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Cyclosporine suppliers with KDMF on PharmaCompass.
We have 8 companies offering Cyclosporine
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