01 1Joyang Laboratories
01 1Daeshin Muyak Co., Ltd.
01 1bacitracin zinc
01 1China
Registrant Name : Daeshin Muyak Co., Ltd.
Registration Date : 2026-04-15
Registration Number : 20260415-211-J-2160
Manufacturer Name : Joyang Laboratories
Manufacturer Address : No.9 Haidu North Road, Sheyang Economic Development Zone
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PharmaCompass offers a list of Bacitracin Zinc 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 Bacitracin Zinc manufacturer or Bacitracin Zinc supplier for your needs.
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A Bacitracin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Bacitracin, including repackagers and relabelers. The FDA regulates Bacitracin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Bacitracin 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 Bacitracin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Bacitracin supplier is an individual or a company that provides Bacitracin active pharmaceutical ingredient (API) or Bacitracin finished formulations upon request. The Bacitracin suppliers may include Bacitracin API manufacturers, exporters, distributors and traders.
click here to find a list of Bacitracin 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 Bacitracin Drug Master File in Korea (Bacitracin KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Bacitracin. The MFDS reviews the Bacitracin KDMF as part of the drug registration process and uses the information provided in the Bacitracin KDMF to evaluate the safety and efficacy of the drug.
After submitting a Bacitracin 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 Bacitracin API can apply through the Korea Drug Master File (KDMF).
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