01 3Solara Active Pharma Sciences Limited
02 1Vifor(International) AG
01 1Aging Life Science Co., Ltd.
02 1Fresenius Medical Care Korea Co., Ltd.
03 1Lihu Healthcare Co., Ltd.
04 1Masung LS Co., Ltd.
01 4sucroferric oxyhydroxide
01 3India
02 1Switzerland
Registrant Name : Fresenius Medical Care Korea Co., Ltd.
Registration Date : 2018-03-19
Registration Number : Su539-1-ND
Manufacturer Name : Vifor(International) AG
Manufacturer Address : Rechenstrasse 37, 9014 St. Gallen, Switzerland
Registrant Name : Lihu Healthcare Co., Ltd.
Registration Date : 2024-07-25
Registration Number : No. 163-34-ND(B)
Manufacturer Name : Solara Active Pharma Science...
Manufacturer Address : A1/B, Sipcot Industrial Complex, Kudikadu, Cuddalore 607 005, India
Registrant Name : Aging Life Science Co., Ltd.
Registration Date : 2024-05-31
Registration Number : No. 163-34-ND(A)
Manufacturer Name : Solara Active Pharma Science...
Manufacturer Address : A1/B, Sipcot Industrial Complex, Kudikadu, Cuddalore 607 005, India
Registrant Name : Masung LS Co., Ltd.
Registration Date : 2024-04-30
Registration Number : 163-34-ND
Manufacturer Name : Solara Active Pharma Science...
Manufacturer Address : A1/B, SIPCOT Industrial Complex, Kudikadu,Cuddalore- 607 005, Tamil Nadu, India
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PharmaCompass offers a list of Sucroferric Oxyhydroxide 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 Sucroferric Oxyhydroxide manufacturer or Sucroferric Oxyhydroxide supplier for your needs.
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PharmaCompass also assists you with knowing the Sucroferric Oxyhydroxide API Price utilized in the formulation of products. Sucroferric Oxyhydroxide API Price is not always fixed or binding as the Sucroferric Oxyhydroxide Price is obtained through a variety of data sources. The Sucroferric Oxyhydroxide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Ferrum Hausmann i.v. manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ferrum Hausmann i.v., including repackagers and relabelers. The FDA regulates Ferrum Hausmann i.v. manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ferrum Hausmann i.v. API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Ferrum Hausmann i.v. supplier is an individual or a company that provides Ferrum Hausmann i.v. active pharmaceutical ingredient (API) or Ferrum Hausmann i.v. finished formulations upon request. The Ferrum Hausmann i.v. suppliers may include Ferrum Hausmann i.v. API manufacturers, exporters, distributors and traders.
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In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Ferrum Hausmann i.v. Drug Master File in Korea (Ferrum Hausmann i.v. KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Ferrum Hausmann i.v.. The MFDS reviews the Ferrum Hausmann i.v. KDMF as part of the drug registration process and uses the information provided in the Ferrum Hausmann i.v. KDMF to evaluate the safety and efficacy of the drug.
After submitting a Ferrum Hausmann i.v. 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 Ferrum Hausmann i.v. API can apply through the Korea Drug Master File (KDMF).
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