01 2ARCHIMICA S.P.A Lodi IT
02 1ASAHI KASEI FINECHEM CO., LTD. Osaka JP
03 1MAC CHEM PRODUCTS (INDIA) PVT. LTD. Mumbai IN
04 1Zhejiang Hisun Pharmaceutical Co., Ltd. Taizhou City CN
01 4Cytarabine
02 1Cytarabine, Process 2
01 1China
02 1India
03 2Italy
04 1Japan
01 4Valid
02 1Withdrawn by Holder
Certificate Number : CEP 2023-289 - Rev 00
Status : Valid
Issue Date : 2024-02-06
Type : Chemical
Substance Number : 760
Certificate Number : R1-CEP 2000-048 - Rev 04
Status : Valid
Issue Date : 2020-10-16
Type : Chemical
Substance Number : 760
Certificate Number : CEP 2017-218 - Rev 03
Status : Valid
Issue Date : 2024-09-20
Type : Chemical
Substance Number : 760
Certificate Number : CEP 2012-251 - Rev 02
Status : Valid
Issue Date : 2024-04-30
Type : Chemical
Substance Number : 760
Certificate Number : R1-CEP 2001-390 - Rev 03
Status : Withdrawn by Holder
Issue Date : 2016-08-02
Type : Chemical
Substance Number : 760
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PharmaCompass offers a list of Cytarabine 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 Cytarabine manufacturer or Cytarabine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Cytarabine manufacturer or Cytarabine supplier.
PharmaCompass also assists you with knowing the Cytarabine API Price utilized in the formulation of products. Cytarabine API Price is not always fixed or binding as the Cytarabine Price is obtained through a variety of data sources. The Cytarabine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Cytarabine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cytarabine, including repackagers and relabelers. The FDA regulates Cytarabine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cytarabine 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 Cytarabine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cytarabine supplier is an individual or a company that provides Cytarabine active pharmaceutical ingredient (API) or Cytarabine finished formulations upon request. The Cytarabine suppliers may include Cytarabine API manufacturers, exporters, distributors and traders.
click here to find a list of Cytarabine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Cytarabine CEP of the European Pharmacopoeia monograph is often referred to as a Cytarabine Certificate of Suitability (COS). The purpose of a Cytarabine CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Cytarabine EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Cytarabine to their clients by showing that a Cytarabine CEP has been issued for it. The manufacturer submits a Cytarabine CEP (COS) as part of the market authorization procedure, and it takes on the role of a Cytarabine CEP holder for the record. Additionally, the data presented in the Cytarabine CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Cytarabine DMF.
A Cytarabine CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Cytarabine 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 Cytarabine suppliers with CEP (COS) on PharmaCompass.
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