01 2Joyang Laboratories
01 1Aging Life Science Co., Ltd.
02 1Daeshin Muyak Co., Ltd.
01 2Fusidic acid
01 2China
Registrant Name : Daeshin Muyak Co., Ltd.
Registration Date : 2024-10-07
Registration Number : 20240205-211-J-1605(1)
Manufacturer Name : Joyang Laboratories
Manufacturer Address : No.9, Haidu North Road, Sheyang Economic Development Zone
Registrant Name : Aging Life Science Co., Ltd.
Registration Date : 2024-02-05
Registration Number : 20240205-211-J-1605
Manufacturer Name : Joyang Laboratories
Manufacturer Address : No.9, Haidu North Road, Sheyang Economic Development Zone
97
PharmaCompass offers a list of Fusidic Acid 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 Fusidic Acid manufacturer or Fusidic Acid supplier for your needs.
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A Fucithalmic manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fucithalmic, including repackagers and relabelers. The FDA regulates Fucithalmic manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fucithalmic 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 Fucithalmic manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Fucithalmic supplier is an individual or a company that provides Fucithalmic active pharmaceutical ingredient (API) or Fucithalmic finished formulations upon request. The Fucithalmic suppliers may include Fucithalmic API manufacturers, exporters, distributors and traders.
click here to find a list of Fucithalmic 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 Fucithalmic Drug Master File in Korea (Fucithalmic KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Fucithalmic. The MFDS reviews the Fucithalmic KDMF as part of the drug registration process and uses the information provided in the Fucithalmic KDMF to evaluate the safety and efficacy of the drug.
After submitting a Fucithalmic 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 Fucithalmic API can apply through the Korea Drug Master File (KDMF).
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