01 1Divi's Laboratories Ltd.
02 2GE Healthcare AS
03 1GE Healthcare AS, Lindesnes Site
04 1Jiangxi Brother Pharmaceutical Co., Ltd.
05 1MFC Co., Ltd. @ [First Law Manufacturing Plant] KPX Life Science
06 1Zhejiang Haizhou Pharmaceutical Co., Ltd
07 1Zhejiang Haizhou Pharmaceutical Co., Ltd.
08 1Zhejiang Hichi Pharmaceutical Corporation Limited
09 4Zhejiang Starry Pharmaceutical Co., Ltd.
10 2Zhejiang Taizhou Hisyn Pharmacetical Co.,Ltd.
11 4Zhejiang Taizhou Hisyn Pharmaceutical Co., Ltd.
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PharmaCompass offers a list of Iohexol 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 Iohexol manufacturer or Iohexol supplier for your needs.
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A CAS-66108-95-0 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CAS-66108-95-0, including repackagers and relabelers. The FDA regulates CAS-66108-95-0 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CAS-66108-95-0 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 CAS-66108-95-0 supplier is an individual or a company that provides CAS-66108-95-0 active pharmaceutical ingredient (API) or CAS-66108-95-0 finished formulations upon request. The CAS-66108-95-0 suppliers may include CAS-66108-95-0 API manufacturers, exporters, distributors and traders.
click here to find a list of CAS-66108-95-0 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 CAS-66108-95-0 Drug Master File in Korea (CAS-66108-95-0 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of CAS-66108-95-0. The MFDS reviews the CAS-66108-95-0 KDMF as part of the drug registration process and uses the information provided in the CAS-66108-95-0 KDMF to evaluate the safety and efficacy of the drug.
After submitting a CAS-66108-95-0 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 CAS-66108-95-0 API can apply through the Korea Drug Master File (KDMF).
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