01 1Glenmark Life Sciences Limited.
02 1ORIL Industry
01 1Korea Serviette Co., Ltd.
02 1Sangjin Corporation
01 2Perindopril tertiary butylamine
01 1France
02 1India
Perindopril tertiary butylamine
Registrant Name : Sangjin Corporation
Registration Date : 2021-05-04
Registration Number : 20210504-209-J-856
Manufacturer Name : Glenmark Life Sciences Limit...
Manufacturer Address : Plot No 3109, GIDC Industrial Estate, Ankleshwar - 393 002, Dist. Bharuch, Gujarat St...
Perindopril tertiary butylamine
Registrant Name : Korea Serviette Co., Ltd.
Registration Date : 2022-01-03
Registration Number : 20220103-209-J-1190
Manufacturer Name : ORIL Industry
Manufacturer Address : 13, rue Auguste Desgenétais, BP 17, BOLBEC, 76210, France
A Perindopril Erbumine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Perindopril Erbumine, including repackagers and relabelers. The FDA regulates Perindopril Erbumine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Perindopril Erbumine 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 Perindopril Erbumine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Perindopril Erbumine supplier is an individual or a company that provides Perindopril Erbumine active pharmaceutical ingredient (API) or Perindopril Erbumine finished formulations upon request. The Perindopril Erbumine suppliers may include Perindopril Erbumine API manufacturers, exporters, distributors and traders.
click here to find a list of Perindopril Erbumine 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 Perindopril Erbumine Drug Master File in Korea (Perindopril Erbumine KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Perindopril Erbumine. The MFDS reviews the Perindopril Erbumine KDMF as part of the drug registration process and uses the information provided in the Perindopril Erbumine KDMF to evaluate the safety and efficacy of the drug.
After submitting a Perindopril Erbumine 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 Perindopril Erbumine API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Perindopril Erbumine suppliers with KDMF on PharmaCompass.
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