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 23239-88-5 (hydrochloride) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 23239-88-5 (hydrochloride), including repackagers and relabelers. The FDA regulates 23239-88-5 (hydrochloride) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 23239-88-5 (hydrochloride) 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 23239-88-5 (hydrochloride) manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A 23239-88-5 (hydrochloride) supplier is an individual or a company that provides 23239-88-5 (hydrochloride) active pharmaceutical ingredient (API) or 23239-88-5 (hydrochloride) finished formulations upon request. The 23239-88-5 (hydrochloride) suppliers may include 23239-88-5 (hydrochloride) API manufacturers, exporters, distributors and traders.
click here to find a list of 23239-88-5 (hydrochloride) 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 23239-88-5 (hydrochloride) Drug Master File in Korea (23239-88-5 (hydrochloride) KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of 23239-88-5 (hydrochloride). The MFDS reviews the 23239-88-5 (hydrochloride) KDMF as part of the drug registration process and uses the information provided in the 23239-88-5 (hydrochloride) KDMF to evaluate the safety and efficacy of the drug.
After submitting a 23239-88-5 (hydrochloride) 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 23239-88-5 (hydrochloride) API can apply through the Korea Drug Master File (KDMF).
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