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.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Desonide manufacturer or Desonide supplier.
A Desonida manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Desonida, including repackagers and relabelers. The FDA regulates Desonida manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Desonida 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 Desonida manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Desonida supplier is an individual or a company that provides Desonida active pharmaceutical ingredient (API) or Desonida finished formulations upon request. The Desonida suppliers may include Desonida API manufacturers, exporters, distributors and traders.
click here to find a list of Desonida 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 Desonida Drug Master File in Korea (Desonida KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Desonida. The MFDS reviews the Desonida KDMF as part of the drug registration process and uses the information provided in the Desonida KDMF to evaluate the safety and efficacy of the drug.
After submitting a Desonida 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 Desonida API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Desonida suppliers with KDMF on PharmaCompass.
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