01 2Eastman Chemical Company
01 1Dong-A ST Co., Ltd.
02 1Sungwoo Chemical Co., Ltd.
01 2Hydroquinone
01 2U.S.A
Registrant Name : Dong-A ST Co., Ltd.
Registration Date : 2024-06-20
Registration Number : 20240620-211-J-1657
Manufacturer Name : Eastman Chemical Company
Manufacturer Address : 200 South Wilcox Drive, Kingsport, TN 37660, USA
Registrant Name : Sungwoo Chemical Co., Ltd.
Registration Date : 2024-09-04
Registration Number : 20240620-211-J-1657(1)
Manufacturer Name : Eastman Chemical Company
Manufacturer Address : 200 South Wilcox Drive, Kingsport, TN 37660, USA
A Hydroquinone manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Hydroquinone, including repackagers and relabelers. The FDA regulates Hydroquinone manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Hydroquinone 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 Hydroquinone manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Hydroquinone supplier is an individual or a company that provides Hydroquinone active pharmaceutical ingredient (API) or Hydroquinone finished formulations upon request. The Hydroquinone suppliers may include Hydroquinone API manufacturers, exporters, distributors and traders.
click here to find a list of Hydroquinone 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 Hydroquinone Drug Master File in Korea (Hydroquinone KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Hydroquinone. The MFDS reviews the Hydroquinone KDMF as part of the drug registration process and uses the information provided in the Hydroquinone KDMF to evaluate the safety and efficacy of the drug.
After submitting a Hydroquinone 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 Hydroquinone API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Hydroquinone suppliers with KDMF on PharmaCompass.
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