01 2Hi-Tech Farm Co., Ltd.
02 1Zhuhai United Laboratories Co., Ltd.
01 2Hi-Tech Farm Co., Ltd.
02 1JDW Pharmaceutical Co., Ltd.
01 3Imipenem hydrate
01 1South 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 : JDW Pharmaceutical Co., Ltd.
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, 1Ma 301, Sihwa Industrial Complex (Jeongwang...
A Imipenem manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Imipenem, including repackagers and relabelers. The FDA regulates Imipenem manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Imipenem 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 Imipenem manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Imipenem supplier is an individual or a company that provides Imipenem active pharmaceutical ingredient (API) or Imipenem finished formulations upon request. The Imipenem suppliers may include Imipenem API manufacturers, exporters, distributors and traders.
click here to find a list of Imipenem 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 Imipenem Drug Master File in Korea (Imipenem KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Imipenem. The MFDS reviews the Imipenem KDMF as part of the drug registration process and uses the information provided in the Imipenem KDMF to evaluate the safety and efficacy of the drug.
After submitting a Imipenem 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 Imipenem API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Imipenem suppliers with KDMF on PharmaCompass.
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