01 1AKUMS LIFESCIENCES LIMITED Mohali District IN
02 1HANMI FINE CHEMICAL CO., LTD. Siheung-si KR
03 1JEIL PHARMACEUTICAL CO., LTD. Yongin-si KR
04 1NECTAR LIFESCIENCES LIMITED Tehsil Dera Bassi IN
05 3Qilu Antibiotics Pharmaceutical Co., Ltd. Jinan CN
06 1Ranbaxy Laboratories Limited Gurgaon IN
07 1SANDOZ GMBH Kundl AT
08 1SANDOZ PRIVATE LIMITED Navi Mumbai IN
01 7Cefpodoxime proxetil
02 1Cefpodoxime proxetil, Process 2
03 1Cefpodoxime proxetil, Process 3
04 1Cefpodoxime proxetil, Turbhe site
01 3China
02 2Germany
03 3India
04 2South Korea
01 7Valid
02 3Withdrawn by Holder
Certificate Number : R1-CEP 2011-165 - Rev 01
Status : Valid
Issue Date : 2021-12-13
Type : Chemical
Substance Number : 2341
Certificate Number : R0-CEP 2012-166 - Rev 02
Status : Withdrawn by Holder
Issue Date : 2016-06-22
Type : Chemical
Substance Number : 2341
Certificate Number : R1-CEP 2015-146 - Rev 00
Status : Valid
Issue Date : 2022-04-14
Type : Chemical
Substance Number : 2341
Certificate Number : R1-CEP 2015-354 - Rev 00
Status : Valid
Issue Date : 2022-08-01
Type : Chemical
Substance Number : 2341
Cefpodoxime Proxetil, Process 3
Certificate Number : R0-CEP 2020-399 - Rev 00
Status : Valid
Issue Date : 2021-03-15
Type : Chemical
Substance Number : 2341
Certificate Number : CEP 2017-030 - Rev 01
Status : Valid
Issue Date : 2023-10-09
Type : Chemical
Substance Number : 2341
Cefpodoxime Proxetil, Process 2
Certificate Number : R0-CEP 2019-319 - Rev 00
Status : Valid
Issue Date : 2020-09-21
Type : Chemical
Substance Number : 2341
Certificate Number : R0-CEP 2010-186 - Rev 01
Status : Withdrawn by Holder
Issue Date : 2013-08-08
Type : Chemical
Substance Number : 2341
Certificate Number : R1-CEP 2010-283 - Rev 01
Status : Valid
Issue Date : 2017-12-05
Type : Chemical
Substance Number : 2341
Cefpodoxime Proxetil, Turbhe Site
Certificate Number : R0-CEP 2013-064 - Rev 00
Status : Withdrawn by Holder
Issue Date : 2013-09-30
Type : Chemical
Substance Number : 2341
A CAS-87239-81-4 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CAS-87239-81-4, including repackagers and relabelers. The FDA regulates CAS-87239-81-4 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CAS-87239-81-4 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 CAS-87239-81-4 supplier is an individual or a company that provides CAS-87239-81-4 active pharmaceutical ingredient (API) or CAS-87239-81-4 finished formulations upon request. The CAS-87239-81-4 suppliers may include CAS-87239-81-4 API manufacturers, exporters, distributors and traders.
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A CAS-87239-81-4 CEP of the European Pharmacopoeia monograph is often referred to as a CAS-87239-81-4 Certificate of Suitability (COS). The purpose of a CAS-87239-81-4 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of CAS-87239-81-4 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of CAS-87239-81-4 to their clients by showing that a CAS-87239-81-4 CEP has been issued for it. The manufacturer submits a CAS-87239-81-4 CEP (COS) as part of the market authorization procedure, and it takes on the role of a CAS-87239-81-4 CEP holder for the record. Additionally, the data presented in the CAS-87239-81-4 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the CAS-87239-81-4 DMF.
A CAS-87239-81-4 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. CAS-87239-81-4 CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
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