01 1Bayer AG
02 1Divi's Laboratories Limited (Unit I)
01 2Bayer Korea Co., Ltd.
01 1Iopromid
02 1Iopromide
01 1Germany
02 1India
Registrant Name : Bayer Korea Co., Ltd.
Registration Date : 2018-07-06
Registration Number : 20180706-210-J-240
Manufacturer Name : Bayer AG
Manufacturer Address : Ernst-Schering-Straße 14 59192 Bergkamen Germany
Registrant Name : Bayer Korea Co., Ltd.
Registration Date : 2026-04-15
Registration Number : 20260415-210-J-2176
Manufacturer Name : Divi's Laboratories Limited ...
Manufacturer Address : Lingojigudem Village, Choutuppal Mandal Yadadri Bhuvanagiri District, Telangana 50825...
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PharmaCompass offers a list of Iopromide 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 Iopromide manufacturer or Iopromide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Iopromide manufacturer or Iopromide supplier.
A Iopromida manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Iopromida, including repackagers and relabelers. The FDA regulates Iopromida manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Iopromida 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 Iopromida manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Iopromida supplier is an individual or a company that provides Iopromida active pharmaceutical ingredient (API) or Iopromida finished formulations upon request. The Iopromida suppliers may include Iopromida API manufacturers, exporters, distributors and traders.
click here to find a list of Iopromida 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 Iopromida Drug Master File in Korea (Iopromida KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Iopromida. The MFDS reviews the Iopromida KDMF as part of the drug registration process and uses the information provided in the Iopromida KDMF to evaluate the safety and efficacy of the drug.
After submitting a Iopromida 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 Iopromida API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Iopromida suppliers with KDMF on PharmaCompass.
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