01 1Shiono Finesse, Ltd. (Fukui Factory)@Kissei Pharmaceutical Co.,Ltd. (Matsumoto Plant)
01 1JDW Pharmaceutical Co., Ltd.
01 1Ozagrel hydrochloride monohydrate
01 1Japan
Ozagrel hydrochloride monohydrate
Registrant Name : JDW Pharmaceutical Co., Ltd.
Registration Date : 2022-09-21
Registration Number : 20220921-209-J-1366
Manufacturer Name : Shiono Finesse, Ltd. (Fukui ...
Manufacturer Address : 156-1 Aza-hamawari, Yonozu 49, Mikuni-cho, Sakai, Fukui, Japan@19-48, Yoshino, Matsum...
A Ozagrel Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ozagrel Hydrochloride, including repackagers and relabelers. The FDA regulates Ozagrel Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ozagrel 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 Ozagrel Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ozagrel Hydrochloride supplier is an individual or a company that provides Ozagrel Hydrochloride active pharmaceutical ingredient (API) or Ozagrel Hydrochloride finished formulations upon request. The Ozagrel Hydrochloride suppliers may include Ozagrel Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Ozagrel Hydrochloride 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 Ozagrel Hydrochloride Drug Master File in Korea (Ozagrel Hydrochloride KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Ozagrel Hydrochloride. The MFDS reviews the Ozagrel Hydrochloride KDMF as part of the drug registration process and uses the information provided in the Ozagrel Hydrochloride KDMF to evaluate the safety and efficacy of the drug.
After submitting a Ozagrel 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 Ozagrel Hydrochloride API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Ozagrel Hydrochloride suppliers with KDMF on PharmaCompass.
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