01 ARCHIMICA S.P.A Lodi IT (2)
02 ASAHI KASEI FINECHEM CO., LTD. Osaka JP (1)
03 Ferro Pfanstiehl Laboratories Inc Waukegan US (1)
04 MAC CHEM PRODUCTS (INDIA) PVT. LTD. Mumbai IN (1)
05 Zhejiang Hisun Pharmaceutical Co., Ltd. Taizhou City CN (1)
01 Cytarabine (5)
02 Cytarabine, Process 2 (1)
01 China (1)
02 India (1)
03 Italy (2)
04 Japan (1)
05 U.S.A (1)
01 Suspended by EDQM GMP non-compliance (1)
02 Valid (3)
03 Withdrawn by Holder (2)
30
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.
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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 MolPort-001-792-509 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MolPort-001-792-509, including repackagers and relabelers. The FDA regulates MolPort-001-792-509 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MolPort-001-792-509 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 MolPort-001-792-509 supplier is an individual or a company that provides MolPort-001-792-509 active pharmaceutical ingredient (API) or MolPort-001-792-509 finished formulations upon request. The MolPort-001-792-509 suppliers may include MolPort-001-792-509 API manufacturers, exporters, distributors and traders.
click here to find a list of MolPort-001-792-509 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A MolPort-001-792-509 CEP of the European Pharmacopoeia monograph is often referred to as a MolPort-001-792-509 Certificate of Suitability (COS). The purpose of a MolPort-001-792-509 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of MolPort-001-792-509 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of MolPort-001-792-509 to their clients by showing that a MolPort-001-792-509 CEP has been issued for it. The manufacturer submits a MolPort-001-792-509 CEP (COS) as part of the market authorization procedure, and it takes on the role of a MolPort-001-792-509 CEP holder for the record. Additionally, the data presented in the MolPort-001-792-509 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the MolPort-001-792-509 DMF.
A MolPort-001-792-509 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. MolPort-001-792-509 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 MolPort-001-792-509 suppliers with CEP (COS) on PharmaCompass.
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