01 1AKUMS LIFESCIENCES LIMITED Mohali District IN
02 1APITORIA PHARMA PRIVATE LIMITED Hyderabad IN
03 1COVALENT LABORATORIES PRIVATE LIMITED Hyderabad IN
04 1DAEWOONG BIO INC. Hwasung-City KR
05 1DHANUKA LABORATORIES LTD. Gurgaon IN
06 1Deva Holding Inc. Cerkezköy / Tekirdag TR
07 1Fako Ilaçlari A.S. Istanbul TR
08 1GlaxoSmithKline Research & Development Limited Brentford GB
09 1Kukje Pharmaceutical Ind. Co., Ltd. Seongnam-City KR
10 2NECTAR LIFESCIENCES LIMITED Tehsil Dera Bassi IN
11 2ORCHID PHARMA LIMITED Alathur IN
12 1Ranbaxy Laboratories Limited Gurgaon IN
13 1SANDOZ PRIVATE LIMITED Navi Mumbai IN
14 1SUN PHARMACEUTICAL INDUSTRIES LIMITED Mumbai IN
15 1SURYA PHARMACEUTICAL LTD. Chandigarh IN
16 1TITAN PHARMACEUTICAL CO., LTD. (GUANGDONG) Heyuan City CN
17 1UNIMARK REMEDIES LIMITED Mumbai IN
18 1Wockhardt Limited Mumbai IN
19 1ZHEJIANG DONGYING PHARMACEUTICAL CO., LTD. Shaoxing CN
01 11Cefuroxime axetil
02 7Cefuroxime axetil, Amorphous
03 1Cefuroxime axetil, Amorphous, Process-II
04 1Cefuroxime axetil, Enzymatic process
05 1Cefuroxime axetil, amorphous
01 2China
02 1Germany
03 13India
04 2South Korea
05 2Turkey
06 1United Kingdom
01 2Expired
02 1Suspended by Holder
03 13Valid
04 2Withdrawn by EDQM Failure to CEP procedure
05 3Withdrawn by Holder
Certificate Number : R1-CEP 2008-203 - Rev 01
Status : Valid
Issue Date : 2022-01-10
Type : Chemical
Substance Number : 1300
Certificate Number : CEP 2011-172 - Rev 03
Status : Valid
Issue Date : 2024-10-02
Type : Chemical
Substance Number : 1300
Certificate Number : R1-CEP 2003-114 - Rev 00
Status : Valid
Issue Date : 2011-02-04
Type : Chemical
Substance Number : 1300
Cefuroxime Axetil, Amorphous, Process-II
Certificate Number : R1-CEP 2016-170 - Rev 01
Status : Valid
Issue Date : 2022-01-17
Type : Chemical
Substance Number : 1300
Certificate Number : CEP 2009-045 - Rev 03
Status : Valid
Issue Date : 2024-04-24
Type : Chemical
Substance Number : 1300
Cefuroxime Axetil, Enzymatic Process
Certificate Number : CEP 2010-206 - Rev 04
Status : Valid
Issue Date : 2024-10-14
Type : Chemical
Substance Number : 1300
Certificate Number : CEP 2002-114 - Rev 04
Status : Valid
Issue Date : 2024-09-06
Type : Chemical
Substance Number : 1300
Certificate Number : R1-CEP 2001-353 - Rev 05
Status : Valid
Issue Date : 2022-08-17
Type : Chemical
Substance Number : 1300
Certificate Number : R1-CEP 2017-034 - Rev 00
Status : Valid
Issue Date : 2023-04-20
Type : Chemical
Substance Number : 1300
Certificate Number : CEP 2023-149 - Rev 00
Status : Valid
Issue Date : 2024-09-04
Type : Chemical
Substance Number : 1300
A Cefuroxime Axetil manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cefuroxime Axetil, including repackagers and relabelers. The FDA regulates Cefuroxime Axetil manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cefuroxime Axetil 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 Cefuroxime Axetil manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cefuroxime Axetil supplier is an individual or a company that provides Cefuroxime Axetil active pharmaceutical ingredient (API) or Cefuroxime Axetil finished formulations upon request. The Cefuroxime Axetil suppliers may include Cefuroxime Axetil API manufacturers, exporters, distributors and traders.
click here to find a list of Cefuroxime Axetil suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Cefuroxime Axetil CEP of the European Pharmacopoeia monograph is often referred to as a Cefuroxime Axetil Certificate of Suitability (COS). The purpose of a Cefuroxime Axetil CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Cefuroxime Axetil EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Cefuroxime Axetil to their clients by showing that a Cefuroxime Axetil CEP has been issued for it. The manufacturer submits a Cefuroxime Axetil CEP (COS) as part of the market authorization procedure, and it takes on the role of a Cefuroxime Axetil CEP holder for the record. Additionally, the data presented in the Cefuroxime Axetil CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Cefuroxime Axetil DMF.
A Cefuroxime Axetil CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Cefuroxime Axetil 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 Cefuroxime Axetil suppliers with CEP (COS) on PharmaCompass.
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