01 1ALP Pharm
02 2Bayer AG
03 1BrightGene Bio-Medical Technology Co.,Ltd
04 1Brother Enterprises Holding
05 1Daewoong Pharmaceutical
06 2Divis Laboratories
07 1JRC
08 1Sichuan Renan Pharmaceutical
09 1Xian Wanlong Pharmaceutical Co. Ltd
10 1Zhejiang Starry Pharmaceutical Co., Ltd
01 6China
02 2Germany
03 3India
04 1South Korea
01 3Active
02 1Inactive
03 8Blank
01 3Valid
02 9Blank
01 1221MF10003
02 11Blank
01 1WC-0031
02 1WC-0031A3
03 10Blank
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GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 8178
Submission : 1989-08-15
Status : Active
Type : II
Certificate Number : R0-CEP 2020-273 - Rev 00
Issue Date : 2021-01-06
Type : Chemical
Substance Number : 1753
Status : Valid
Registration Number : 221MF10003
Registrant's Address : Kaiser-Wilhelm-Allee 1,51373 Leverkusen, Germany
Initial Date of Registration : 2009-01-13
Latest Date of Registration : --
Registrant Name : Bayer Korea 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
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 38239
Submission : 2023-04-09
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 35356
Submission : 2020-12-04
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 25680
Submission : 2012-01-05
Status : Inactive
Type : II
Certificate Number : CEP 2022-232 - Rev 00
Issue Date : 2024-07-16
Type : Chemical
Substance Number : 1753
Status : Valid
Certificate Number : R1-CEP 2015-172 - Rev 00
Issue Date : 2022-01-31
Type : Chemical
Substance Number : 1753
Status : Valid
Registrant Name : Bayer Korea 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
Date of Issue : 2022-06-16
Valid Till : 2025-06-16
Written Confirmation Number : WC-0031
Address of the Firm :
Date of Issue : 2020-12-18
Valid Till : 2022-06-16
Written Confirmation Number : WC-0031A3
Address of the Firm :
A Iopromide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Iopromide, including repackagers and relabelers. The FDA regulates Iopromide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Iopromide 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 Iopromide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Iopromide supplier is an individual or a company that provides Iopromide active pharmaceutical ingredient (API) or Iopromide finished formulations upon request. The Iopromide suppliers may include Iopromide API manufacturers, exporters, distributors and traders.
click here to find a list of Iopromide suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
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