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