01 1Asence Pharma Private Limited Vadodara IN
02 1North China Pharmaceutical Huasheng Co., Ltd. Shijiazhuang CN
03 1XELLIA PHARMACEUTICALS APS Copenhagen S DK
04 2ZHEJIANG TIANTAI PHARMACEUTICAL CO., LTD. Taizhou City CN
01 2Amphotericin B
02 1Amphotericin B, Intended For Use in the Manufacture of Parenteral Preparations
03 1Amphotericin B, Process I
04 1Amphotericin B, Process II, for use in the manufacture of parenteral preparations
01 3China
02 1Denmark
03 1Blank
01 5Valid
Amphotericin B, Intended For Use In The Manufact...
Certificate Number : CEP 2024-118 - Rev 00
Status : Valid
Issue Date : 2025-06-13
Type : Chemical
Substance Number : 1292
Certificate Number : R1-CEP 2005-212 - Rev 04
Status : Valid
Issue Date : 2023-08-17
Type : Chemical
Substance Number : 1292
Certificate Number : R1-CEP 2002-079 - Rev 09
Status : Valid
Issue Date : 2023-05-12
Type : Chemical
Substance Number : 1292
Certificate Number : CEP 2023-150 - Rev 01
Status : Valid
Issue Date : 2025-05-14
Type : Chemical
Substance Number : 1292
Amphotericin B, Process II, For Use In The Manuf...
Certificate Number : CEP 2023-152 - Rev 00
Status : Valid
Issue Date : 2024-07-03
Type : Chemical
Substance Number : 1292
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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.
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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 C-AmB manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of C-AmB, including repackagers and relabelers. The FDA regulates C-AmB manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. C-AmB 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 C-AmB manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A C-AmB supplier is an individual or a company that provides C-AmB active pharmaceutical ingredient (API) or C-AmB finished formulations upon request. The C-AmB suppliers may include C-AmB API manufacturers, exporters, distributors and traders.
click here to find a list of C-AmB suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A C-AmB CEP of the European Pharmacopoeia monograph is often referred to as a C-AmB Certificate of Suitability (COS). The purpose of a C-AmB CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of C-AmB EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of C-AmB to their clients by showing that a C-AmB CEP has been issued for it. The manufacturer submits a C-AmB CEP (COS) as part of the market authorization procedure, and it takes on the role of a C-AmB CEP holder for the record. Additionally, the data presented in the C-AmB CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the C-AmB DMF.
A C-AmB CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. C-AmB CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of C-AmB suppliers with CEP (COS) on PharmaCompass.
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