01 1Pfizer Ireland Pharmaceuticals
01 1Beatrice Korea Co., Ltd.
01 1Ziprasidone hydrochloride monohydrate
01 1U.S.A
Ziprasidone hydrochloride monohydrate
Registrant Name : Beatrice Korea Co., Ltd.
Registration Date : 2022-09-06
Registration Number : 20220906-209-J-1358
Manufacturer Name : Pfizer Ireland Pharmaceutica...
Manufacturer Address : Ringaskiddy API Plant, PO Box 140, Ringaskiddy, Co. Cork, Ireland
A Ziprasidone Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ziprasidone Hydrochloride, including repackagers and relabelers. The FDA regulates Ziprasidone Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ziprasidone 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 Ziprasidone Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ziprasidone Hydrochloride supplier is an individual or a company that provides Ziprasidone Hydrochloride active pharmaceutical ingredient (API) or Ziprasidone Hydrochloride finished formulations upon request. The Ziprasidone Hydrochloride suppliers may include Ziprasidone Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Ziprasidone 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 Ziprasidone Hydrochloride Drug Master File in Korea (Ziprasidone Hydrochloride KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Ziprasidone Hydrochloride. The MFDS reviews the Ziprasidone Hydrochloride KDMF as part of the drug registration process and uses the information provided in the Ziprasidone Hydrochloride KDMF to evaluate the safety and efficacy of the drug.
After submitting a Ziprasidone 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 Ziprasidone Hydrochloride API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Ziprasidone Hydrochloride suppliers with KDMF on PharmaCompass.
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