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01 1Daepyeong Co., Ltd.
02 1Hyundai Bioland Co., Ltd.
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01 1Daepyeong Co., Ltd.
02 1Hyundai Bioland Co., Ltd.
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01 2Hyunho-saek·Gyeonwooja (5:1) 50% ethanol soft extract (9.5~11.5→1)
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01 2South Korea
Hyunho-saek·Gyeonwooja (5:1) 50% ethanol soft extract (9.5~11.5→1)
Registrant Name : Daepyeong Co., Ltd.
Registration Date : 2017-12-19
Registration Number : 20171219-13-K-18-01
Manufacturer Name : Daepyeong Co., Ltd.
Manufacturer Address : 19-8 Yeongdong-gil, Hamchang-eup, Sangju-si, Gyeongbuk
Hyunho-saek·Gyeonwooja (5:1) 50% ethanol soft extract (9.5~11.5→1)
Registrant Name : Hyundai Bioland Co., Ltd.
Registration Date : 2018-09-11
Registration Number : 20180911-13-K-41-02
Manufacturer Name : Hyundai Bioland Co., Ltd.
Manufacturer Address : 22 Osong Life 2-ro, Osong-eup, Heungdeok-gu, Cheongju-si, Chungcheongbuk-do
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PharmaCompass offers a list of Rotundine 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 Rotundine manufacturer or Rotundine supplier for your needs.
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A Tetrahydropalmatine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tetrahydropalmatine, including repackagers and relabelers. The FDA regulates Tetrahydropalmatine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tetrahydropalmatine 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 Tetrahydropalmatine supplier is an individual or a company that provides Tetrahydropalmatine active pharmaceutical ingredient (API) or Tetrahydropalmatine finished formulations upon request. The Tetrahydropalmatine suppliers may include Tetrahydropalmatine API manufacturers, exporters, distributors and traders.
click here to find a list of Tetrahydropalmatine 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 Tetrahydropalmatine Drug Master File in Korea (Tetrahydropalmatine KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Tetrahydropalmatine. The MFDS reviews the Tetrahydropalmatine KDMF as part of the drug registration process and uses the information provided in the Tetrahydropalmatine KDMF to evaluate the safety and efficacy of the drug.
After submitting a Tetrahydropalmatine 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 Tetrahydropalmatine API can apply through the Korea Drug Master File (KDMF).
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