01 1MEDIGRAPH PHARMACEUTICALS PRIVATE LIMITED
01 1Daeshin Muyak Co., Ltd.
01 1Prilocaine
01 1India
Registrant Name : Daeshin Muyak Co., Ltd.
Registration Date : 2025-04-04
Registration Number : 20250404-210-J-1829
Manufacturer Name : MEDIGRAPH PHARMACEUTICALS PR...
Manufacturer Address : Plot No. J46/J57, MIDC Taloja, District Raigad, Maharashtra State Raigad 410208, Indi...
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A PRILOCAINE BASE manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of PRILOCAINE BASE, including repackagers and relabelers. The FDA regulates PRILOCAINE BASE manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. PRILOCAINE BASE 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 PRILOCAINE BASE manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A PRILOCAINE BASE supplier is an individual or a company that provides PRILOCAINE BASE active pharmaceutical ingredient (API) or PRILOCAINE BASE finished formulations upon request. The PRILOCAINE BASE suppliers may include PRILOCAINE BASE API manufacturers, exporters, distributors and traders.
click here to find a list of PRILOCAINE BASE 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 PRILOCAINE BASE Drug Master File in Korea (PRILOCAINE BASE KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of PRILOCAINE BASE. The MFDS reviews the PRILOCAINE BASE KDMF as part of the drug registration process and uses the information provided in the PRILOCAINE BASE KDMF to evaluate the safety and efficacy of the drug.
After submitting a PRILOCAINE BASE 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 PRILOCAINE BASE API can apply through the Korea Drug Master File (KDMF).
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