01 1North China Pharmaceutical Huasheng Co., Ltd.
02 2Xellia Pharmaceuticals ApS
01 1DKS Korea Co., Ltd.
02 1Gilead Sciences Korea Ltd.
03 1Hiple Co., Ltd.
01 2Amphoteric Mystery
02 1Amphotericin B
01 1China
02 2Denmark
Registrant Name : Hiple Co., Ltd.
Registration Date : 2023-06-08
Registration Number : 20230608-210-J-1507
Manufacturer Name : North China Pharmaceutical H...
Manufacturer Address : No.8 Yangzi Road, Shijiazhuang Economic & Technological Development Zone, Hebei 05216...
Registrant Name : Gilead Sciences Korea Ltd.
Registration Date : 2020-07-27
Registration Number : 20200727-210-J-391
Manufacturer Name : Xellia Pharmaceuticals ApS
Manufacturer Address : Dalslandsgade 11, Kobenhavn S, 2300 Denmark
Registrant Name : DKS Korea Co., Ltd.
Registration Date : 2020-10-13
Registration Number : 20200727-210-J-391(1)
Manufacturer Name : Xellia Pharmaceuticals ApS
Manufacturer Address : Dalslandsgade 11, Kobenhavn S, 2300 Denmark
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PharmaCompass offers a list of Amphotericin B 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 Amphotericin B manufacturer or Amphotericin B supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Amphotericin B manufacturer or Amphotericin B supplier.
PharmaCompass also assists you with knowing the Amphotericin B API Price utilized in the formulation of products. Amphotericin B API Price is not always fixed or binding as the Amphotericin B Price is obtained through a variety of data sources. The Amphotericin B Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A DB00681 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DB00681, including repackagers and relabelers. The FDA regulates DB00681 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DB00681 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 DB00681 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A DB00681 supplier is an individual or a company that provides DB00681 active pharmaceutical ingredient (API) or DB00681 finished formulations upon request. The DB00681 suppliers may include DB00681 API manufacturers, exporters, distributors and traders.
click here to find a list of DB00681 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 DB00681 Drug Master File in Korea (DB00681 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of DB00681. The MFDS reviews the DB00681 KDMF as part of the drug registration process and uses the information provided in the DB00681 KDMF to evaluate the safety and efficacy of the drug.
After submitting a DB00681 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 DB00681 API can apply through the Korea Drug Master File (KDMF).
click here to find a list of DB00681 suppliers with KDMF on PharmaCompass.
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