01 1Pfizer Ireland Pharmaceuticals
01 1Korea Pfizer Pharmaceutical Co., Ltd.
01 1Iletriptan hydrobromide
01 1U.S.A
Registrant Name : Korea Pfizer Pharmaceutical Co., Ltd.
Registration Date : 2011-12-09
Registration Number : Su189-14-ND
Manufacturer Name : Pfizer Ireland Pharmaceutica...
Manufacturer Address : Ringaskiddy Active Pharmaceutical Ingredient Plant, PO Box 140, Ringaskiddy, Co. Cork...
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PharmaCompass offers a list of Eletriptan Hydrobromide 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 Eletriptan Hydrobromide manufacturer or Eletriptan Hydrobromide supplier for your needs.
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PharmaCompass also assists you with knowing the Eletriptan Hydrobromide API Price utilized in the formulation of products. Eletriptan Hydrobromide API Price is not always fixed or binding as the Eletriptan Hydrobromide Price is obtained through a variety of data sources. The Eletriptan Hydrobromide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Relert manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Relert, including repackagers and relabelers. The FDA regulates Relert manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Relert 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 Relert manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Relert supplier is an individual or a company that provides Relert active pharmaceutical ingredient (API) or Relert finished formulations upon request. The Relert suppliers may include Relert API manufacturers, exporters, distributors and traders.
click here to find a list of Relert 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 Relert Drug Master File in Korea (Relert KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Relert. The MFDS reviews the Relert KDMF as part of the drug registration process and uses the information provided in the Relert KDMF to evaluate the safety and efficacy of the drug.
After submitting a Relert 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 Relert API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Relert suppliers with KDMF on PharmaCompass.
