01 1TOYAMA CHEMICAL CO., LTD.
01 1Hanall Biopharma Co., Ltd.
01 1Pajufloxacin mesylate
01 1Japan
Registrant Name : Hanall Biopharma Co., Ltd.
Registration Date : 2009-07-20
Registration Number : 35-3-ND
Manufacturer Name : TOYAMA CHEMICAL CO., LTD.
Manufacturer Address : 4-1, Shimookui 2-chome, Toyama-city, Toyama, 930-8508
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A 045P414 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 045P414, including repackagers and relabelers. The FDA regulates 045P414 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 045P414 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 045P414 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A 045P414 supplier is an individual or a company that provides 045P414 active pharmaceutical ingredient (API) or 045P414 finished formulations upon request. The 045P414 suppliers may include 045P414 API manufacturers, exporters, distributors and traders.
click here to find a list of 045P414 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 045P414 Drug Master File in Korea (045P414 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of 045P414. The MFDS reviews the 045P414 KDMF as part of the drug registration process and uses the information provided in the 045P414 KDMF to evaluate the safety and efficacy of the drug.
After submitting a 045P414 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 045P414 API can apply through the Korea Drug Master File (KDMF).
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