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