01 1ANHUI POLY PHARM. CO., LTD. Anqing CN
02 1EMCURE PHARMACEUTICALS LIMITED Pune IN
03 1HETERO LABS LIMITED Hyderabad IN
04 1MSN LABORATORIES PRIVATE LIMITED Kardanur Village IN
05 1SHILPA PHARMA LIFESCIENCES LIMITED Raichur IN
06 1Zhejiang Hisun Pharmaceutical Co., Ltd. Taizhou City CN
01 6Cyclophosphamide monohydrate
01 2China
02 4India
01 5Valid
02 1Withdrawn by Holder
Certificate Number : R1-CEP 2010-329 - Rev 02
Status : Valid
Issue Date : 2023-08-24
Type : Chemical
Substance Number : 711
Certificate Number : CEP 2022-356 - Rev 01
Status : Valid
Issue Date : 2024-11-15
Type : Chemical
Substance Number : 711
Certificate Number : R1-CEP 2014-342 - Rev 01
Status : Valid
Issue Date : 2023-06-30
Type : Chemical
Substance Number : 711
Certificate Number : R0-CEP 2018-092 - Rev 01
Status : Valid
Issue Date : 2023-08-23
Type : Chemical
Substance Number : 711
Certificate Number : R0-CEP 2020-083 - Rev 02
Status : Valid
Issue Date : 2023-01-09
Type : Chemical
Substance Number : 711
Certificate Number : R1-CEP 2005-279 - Rev 01
Status : Withdrawn by Holder
Issue Date : 2016-06-30
Type : Chemical
Substance Number : 711
A Cyclophosphamide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cyclophosphamide, including repackagers and relabelers. The FDA regulates Cyclophosphamide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cyclophosphamide 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 Cyclophosphamide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cyclophosphamide supplier is an individual or a company that provides Cyclophosphamide active pharmaceutical ingredient (API) or Cyclophosphamide finished formulations upon request. The Cyclophosphamide suppliers may include Cyclophosphamide API manufacturers, exporters, distributors and traders.
click here to find a list of Cyclophosphamide suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Cyclophosphamide CEP of the European Pharmacopoeia monograph is often referred to as a Cyclophosphamide Certificate of Suitability (COS). The purpose of a Cyclophosphamide CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Cyclophosphamide EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Cyclophosphamide to their clients by showing that a Cyclophosphamide CEP has been issued for it. The manufacturer submits a Cyclophosphamide CEP (COS) as part of the market authorization procedure, and it takes on the role of a Cyclophosphamide CEP holder for the record. Additionally, the data presented in the Cyclophosphamide CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Cyclophosphamide DMF.
A Cyclophosphamide CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Cyclophosphamide 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 Cyclophosphamide suppliers with CEP (COS) on PharmaCompass.
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