01 1Henan Lihua Pharmaceutical Co.,Ltd.
01 1Otran Korea Co., Ltd.
01 1Undifferentiated desonide
01 1China
Registrant Name : Otran Korea Co., Ltd.
Registration Date : 2026-03-12
Registration Number : 20260312-209-J-2144
Manufacturer Name : Henan Lihua Pharmaceutical C...
Manufacturer Address : Qilidian, North part of Antang Road, Longan District, Anyang 455000, China
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PharmaCompass offers a list of Desonide API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Desonide manufacturer or Desonide supplier for your needs.
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A Desone manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Desone, including repackagers and relabelers. The FDA regulates Desone manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Desone 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 Desone manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Desone supplier is an individual or a company that provides Desone active pharmaceutical ingredient (API) or Desone finished formulations upon request. The Desone suppliers may include Desone API manufacturers, exporters, distributors and traders.
click here to find a list of Desone suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 Desone Drug Master File in Korea (Desone KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Desone. The MFDS reviews the Desone KDMF as part of the drug registration process and uses the information provided in the Desone KDMF to evaluate the safety and efficacy of the drug.
After submitting a Desone 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 Desone API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Desone suppliers with KDMF on PharmaCompass.
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