01 1Changzhou Sunlight Pharmaceutical Co., Ltd.
01 1Daeshin Muyak Co., Ltd.
01 1Benzocaine
01 1China
Registrant Name : Daeshin Muyak Co., Ltd.
Registration Date : 2025-06-02
Registration Number : 20250602-211-J-1923
Manufacturer Name : Changzhou Sunlight Pharmaceu...
Manufacturer Address : 216 Yunnan West Road, Benniu Town, Xinbei District, Changzhou City, Jiangsu Province ...
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PharmaCompass offers a list of Benzocaine 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 Benzocaine manufacturer or Benzocaine supplier for your needs.
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A Anaesthesin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Anaesthesin, including repackagers and relabelers. The FDA regulates Anaesthesin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Anaesthesin 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 Anaesthesin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Anaesthesin supplier is an individual or a company that provides Anaesthesin active pharmaceutical ingredient (API) or Anaesthesin finished formulations upon request. The Anaesthesin suppliers may include Anaesthesin API manufacturers, exporters, distributors and traders.
click here to find a list of Anaesthesin 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 Anaesthesin Drug Master File in Korea (Anaesthesin KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Anaesthesin. The MFDS reviews the Anaesthesin KDMF as part of the drug registration process and uses the information provided in the Anaesthesin KDMF to evaluate the safety and efficacy of the drug.
After submitting a Anaesthesin 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 Anaesthesin API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Anaesthesin suppliers with KDMF on PharmaCompass.
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