01 1AbbVie Inc.
02 2CONCORD 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 1North China Pharmaceutical Huasheng Co., Ltd.
08 1Sicor Societa' Italiana Corticosteroidi SRL
09 1Sterling Pharma Ringaskiddy Limited@[Suanfarma Manufacturer] Sandoz GmbH_x000D_ @Suanfarma Italia SpA
10 1TAPI Czech Industries sro@TAPI Hungray Industries Kft.@TAPI Hungray Industries Kft.
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
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PharmaCompass offers a list of Cyclosporine 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 Cyclosporine manufacturer or Cyclosporine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Cyclosporine manufacturer or Cyclosporine supplier.
PharmaCompass also assists you with knowing the Cyclosporine API Price utilized in the formulation of products. Cyclosporine API Price is not always fixed or binding as the Cyclosporine Price is obtained through a variety of data sources. The Cyclosporine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Cyclosporine, United States Pharmacopeia (USP) Reference Standard manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cyclosporine, United States Pharmacopeia (USP) Reference Standard, including repackagers and relabelers. The FDA regulates Cyclosporine, United States Pharmacopeia (USP) Reference Standard manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cyclosporine, United States Pharmacopeia (USP) Reference Standard 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, United States Pharmacopeia (USP) Reference Standard manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cyclosporine, United States Pharmacopeia (USP) Reference Standard supplier is an individual or a company that provides Cyclosporine, United States Pharmacopeia (USP) Reference Standard active pharmaceutical ingredient (API) or Cyclosporine, United States Pharmacopeia (USP) Reference Standard finished formulations upon request. The Cyclosporine, United States Pharmacopeia (USP) Reference Standard suppliers may include Cyclosporine, United States Pharmacopeia (USP) Reference Standard API manufacturers, exporters, distributors and traders.
click here to find a list of Cyclosporine, United States Pharmacopeia (USP) Reference Standard 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, United States Pharmacopeia (USP) Reference Standard Drug Master File in Korea (Cyclosporine, United States Pharmacopeia (USP) Reference Standard KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Cyclosporine, United States Pharmacopeia (USP) Reference Standard. The MFDS reviews the Cyclosporine, United States Pharmacopeia (USP) Reference Standard KDMF as part of the drug registration process and uses the information provided in the Cyclosporine, United States Pharmacopeia (USP) Reference Standard KDMF to evaluate the safety and efficacy of the drug.
After submitting a Cyclosporine, United States Pharmacopeia (USP) Reference Standard 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, United States Pharmacopeia (USP) Reference Standard API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Cyclosporine, United States Pharmacopeia (USP) Reference Standard suppliers with KDMF on PharmaCompass.
We have 9 companies offering Cyclosporine, United States Pharmacopeia (USP) Reference Standard
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