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01 2Hi-Tech Farm Co., Ltd.
02 2Zhuhai United Laboratories Co., Ltd.
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01 2Hi-Tech Farm Co., Ltd.
02 2제이더블유중외제약(주)
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01 1Imipenem
02 3Imipenem hydrate
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01 2South Korea
02 2U.S.A
Registrant Name : Hi-Tech Farm Co., Ltd.
Registration Date : 2018-10-18
Registration Number : 20181018-210-J-345
Manufacturer Name : Hi-Tech Farm Co., Ltd.
Manufacturer Address : 280 Shinnae-ro, Daeso-myeon, Eumseong-gun, Chungcheongbuk-do
Registrant Name : Hi-Tech Farm Co., Ltd.
Registration Date : 2019-10-16
Registration Number : 20191016-210-J-452
Manufacturer Name : Hi-Tech Farm Co., Ltd.
Manufacturer Address : 12, Cheomdansanup 6-ro, Daesowon-myeon, Chungju-si, Chungcheongbuk-do
Registrant Name : 제이더블유중외제약(주)
Registration Date : 2020-07-01
Registration Number : 20200701-210-J-669
Manufacturer Name : Zhuhai United Laboratories C...
Manufacturer Address : 56 Gyeongje-ro, Siheung-si, Gyeonggi-do, Sihwa Industrial Complex 1-ma 301 (Jeongwang...
Registrant Name : 제이더블유중외제약(주)
Registration Date : 2025-03-19
Registration Number : 20250319-210-J-1815
Manufacturer Name : Zhuhai United Laboratories C...
Manufacturer Address : No.2428, Anji Road, Sanzao Town, Jinwan District, Zhuhai, Guangdong 519040, P.R.China
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PharmaCompass offers a list of Imipenem 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 Imipenem manufacturer or Imipenem supplier for your needs.
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A 64221-86-9 (Parent) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 64221-86-9 (Parent), including repackagers and relabelers. The FDA regulates 64221-86-9 (Parent) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 64221-86-9 (Parent) 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 64221-86-9 (Parent) supplier is an individual or a company that provides 64221-86-9 (Parent) active pharmaceutical ingredient (API) or 64221-86-9 (Parent) finished formulations upon request. The 64221-86-9 (Parent) suppliers may include 64221-86-9 (Parent) API manufacturers, exporters, distributors and traders.
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In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a 64221-86-9 (Parent) Drug Master File in Korea (64221-86-9 (Parent) KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of 64221-86-9 (Parent). The MFDS reviews the 64221-86-9 (Parent) KDMF as part of the drug registration process and uses the information provided in the 64221-86-9 (Parent) KDMF to evaluate the safety and efficacy of the drug.
After submitting a 64221-86-9 (Parent) 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 64221-86-9 (Parent) API can apply through the Korea Drug Master File (KDMF).
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