01 1Kyorin Pharmaceutical Group Facilities Co., Ltd. Noshiro Plant
01 1Handok Co., Ltd.
01 1Gatifloxacin 1.5 hydrate
01 1Japan
Registrant Name : Handok Co., Ltd.
Registration Date : 2013-05-07
Registration Number : 20130507-174-I-282-01
Manufacturer Name : Kyorin Pharmaceutical Group ...
Manufacturer Address : 1, Matsubara, Noshiro-shi, Akita, 016-0000, Japan
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PharmaCompass offers a list of Gatifloxacin API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Gatifloxacin manufacturer or Gatifloxacin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Gatifloxacin manufacturer or Gatifloxacin supplier.
PharmaCompass also assists you with knowing the Gatifloxacin API Price utilized in the formulation of products. Gatifloxacin API Price is not always fixed or binding as the Gatifloxacin Price is obtained through a variety of data sources. The Gatifloxacin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Zymer manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Zymer, including repackagers and relabelers. The FDA regulates Zymer manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Zymer 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 Zymer manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Zymer supplier is an individual or a company that provides Zymer active pharmaceutical ingredient (API) or Zymer finished formulations upon request. The Zymer suppliers may include Zymer API manufacturers, exporters, distributors and traders.
click here to find a list of Zymer suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price 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 Zymer Drug Master File in Korea (Zymer KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Zymer. The MFDS reviews the Zymer KDMF as part of the drug registration process and uses the information provided in the Zymer KDMF to evaluate the safety and efficacy of the drug.
After submitting a Zymer 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 Zymer API can apply through the Korea Drug Master File (KDMF).
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