01 1ACS DOBFAR S.P.A. Tribiano IT
02 1FRESENIUS KABI IPSUM S.R.L. Cassina de’ Pecchi IT
03 1Farmabios SpA Gropello Cairoli IT
04 1GlaxoSmithKline Research & Development Limited London GB
05 1Kukje Pharmaceutical Ind Co Ltd Seongnam-City KR
06 1NCPC HEBEI HUAMIN PHARMACEUTICAL CO., LTD. Shijiazhuang CN
07 1NECTAR LIFESCIENCES LIMITED Tehsil Dera Bassi IN
08 2ORCHID PHARMA LIMITED Alathur IN
09 3Qilu Antibiotics Pharmaceutical Co., Ltd. Jinan CN
10 1SANDOZ INDUSTRIAL PRODUCTS GMBH Frankfurt Am Main DE
11 1TITAN PHARMACEUTICAL CO., LTD. (GUANGDONG) Heyuan City CN
12 1Wockhardt Limited Ankleshwar IN
13 1ZHEJIANG DONGYING PHARMACEUTICAL CO., LTD. Shaoxing CN
01 13Cefuroxime sodium, Sterile
02 1Cefuroxime sodium, Sterile, Process 2
03 1Cefuroxime sodium, Sterile, Process 3
04 1Cefuroxime sodium, Sterile, Process II
01 6China
02 1Germany
03 4India
04 3Italy
05 1South Korea
06 1United Kingdom
01 1Suspended by EDQM GMP non-compliance
02 11Valid
03 1Withdrawn by EDQM Failure to CEP procedure
04 3Withdrawn by Holder
Certificate Number : R1-CEP 1996-007 - Rev 05
Status : Valid
Issue Date : 2022-07-25
Type : Chemical
Substance Number : 992
Certificate Number : R1-CEP 1997-044 - Rev 11
Status : Valid
Issue Date : 2021-12-17
Type : Chemical
Substance Number : 992
Certificate Number : CEP 2014-021 - Rev 02
Status : Valid
Issue Date : 2024-01-17
Type : Chemical
Substance Number : 992
Cefuroxime Sodium, Sterile, Process II
Certificate Number : CEP 2021-004 - Rev 01
Status : Valid
Issue Date : 2024-09-09
Type : Chemical
Substance Number : 992
Certificate Number : CEP 2002-086 - Rev 03
Status : Valid
Issue Date : 2024-09-06
Type : Chemical
Substance Number : 992
Cefuroxime Sodium, Sterile, Process 2
Certificate Number : R0-CEP 2020-383 - Rev 00
Status : Valid
Issue Date : 2022-07-08
Type : Chemical
Substance Number : 992
Cefuroxime Sodium, Sterile, Process 3
Certificate Number : CEP 2024-187 - Rev 00
Status : Valid
Issue Date : 2024-11-25
Type : Chemical
Substance Number : 992
Certificate Number : CEP 2006-014 - Rev 03
Status : Valid
Issue Date : 2024-04-30
Type : Chemical
Substance Number : 992
Certificate Number : R1-CEP 2014-335 - Rev 00
Status : Valid
Issue Date : 2022-01-17
Type : Chemical
Substance Number : 992
Certificate Number : CEP 2021-308 - Rev 01
Status : Valid
Issue Date : 2024-10-21
Type : Chemical
Substance Number : 992
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PharmaCompass offers a list of Cefuroxime Sodium 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 Cefuroxime Sodium manufacturer or Cefuroxime Sodium supplier for your needs.
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PharmaCompass also assists you with knowing the Cefuroxime Sodium API Price utilized in the formulation of products. Cefuroxime Sodium API Price is not always fixed or binding as the Cefuroxime Sodium Price is obtained through a variety of data sources. The Cefuroxime Sodium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Cefurex manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cefurex, including repackagers and relabelers. The FDA regulates Cefurex manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cefurex 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 Cefurex manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cefurex supplier is an individual or a company that provides Cefurex active pharmaceutical ingredient (API) or Cefurex finished formulations upon request. The Cefurex suppliers may include Cefurex API manufacturers, exporters, distributors and traders.
click here to find a list of Cefurex suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Cefurex CEP of the European Pharmacopoeia monograph is often referred to as a Cefurex Certificate of Suitability (COS). The purpose of a Cefurex CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Cefurex EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Cefurex to their clients by showing that a Cefurex CEP has been issued for it. The manufacturer submits a Cefurex CEP (COS) as part of the market authorization procedure, and it takes on the role of a Cefurex CEP holder for the record. Additionally, the data presented in the Cefurex CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Cefurex DMF.
A Cefurex CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Cefurex 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 Cefurex suppliers with CEP (COS) on PharmaCompass.
We have 11 companies offering Cefurex
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