01 2Changzhou Pharmaceutical Factory
01 1Boryeong Co., Ltd.
02 1Sampoong Pharmachem Co., Ltd.
01 2Captopril
01 2China
Registrant Name : Sampoong Pharmachem Co., Ltd.
Registration Date : 2021-05-04
Registration Number : 20210504-209-J-977
Manufacturer Name : Changzhou Pharmaceutical Fac...
Manufacturer Address : No.518 Laodong East Road, Changzhou, Jiangsu Province, PR China
Registrant Name : Boryeong Co., Ltd.
Registration Date : 2022-09-19
Registration Number : 20210504-209-J-977(1)
Manufacturer Name : Changzhou Pharmaceutical Fac...
Manufacturer Address : No.518 Laodong East Road, Changzhou, Jiangsu Province, PR China
A Captopril manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Captopril, including repackagers and relabelers. The FDA regulates Captopril manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Captopril 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 Captopril manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Captopril supplier is an individual or a company that provides Captopril active pharmaceutical ingredient (API) or Captopril finished formulations upon request. The Captopril suppliers may include Captopril API manufacturers, exporters, distributors and traders.
click here to find a list of Captopril 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 Captopril Drug Master File in Korea (Captopril KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Captopril. The MFDS reviews the Captopril KDMF as part of the drug registration process and uses the information provided in the Captopril KDMF to evaluate the safety and efficacy of the drug.
After submitting a Captopril 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 Captopril API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Captopril suppliers with KDMF on PharmaCompass.
We have 1 companies offering Captopril
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