01 1ANUH PHARMA LTD. Mumbai IN
02 1ERCROS S.A. Aranjuez ES
03 1SM BIOMED SDN BHD Sungai Petani MY
04 1Sandoz Industrial Products SpA Rovereto IT
01 2Erythromycin ethylsuccinate
02 1Erythromycin ethylsuccinate, Powder, micronised
03 1Erythromycin ethylsuccinate, Pulverised
01 1Germany
02 1India
03 1Malaysia
04 1Spain
01 3Valid
02 1Withdrawn by Holder
Certificate Number : CEP 2007-235 - Rev 08
Status : Valid
Issue Date : 2023-11-14
Type : Chemical
Substance Number : 274
Erythromycin Ethylsuccinate, Powder, Micronised
Certificate Number : CEP 2002-136 - Rev 08
Status : Valid
Issue Date : 2024-12-02
Type : Chemical
Substance Number : 274
Erythromycin Ethylsuccinate, Pulverised
Certificate Number : R1-CEP 1998-046 - Rev 01
Status : Withdrawn by Holder
Issue Date : 2006-05-24
Type : Chemical
Substance Number : 274
Certificate Number : R1-CEP 1999-121 - Rev 04
Status : Valid
Issue Date : 2023-03-08
Type : Chemical
Substance Number : 274
69
PharmaCompass offers a list of Erythromycin Ethyl Succinate 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 Erythromycin Ethyl Succinate manufacturer or Erythromycin Ethyl Succinate supplier for your needs.
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A 1264-62-6 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 1264-62-6, including repackagers and relabelers. The FDA regulates 1264-62-6 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 1264-62-6 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 1264-62-6 supplier is an individual or a company that provides 1264-62-6 active pharmaceutical ingredient (API) or 1264-62-6 finished formulations upon request. The 1264-62-6 suppliers may include 1264-62-6 API manufacturers, exporters, distributors and traders.
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A 1264-62-6 CEP of the European Pharmacopoeia monograph is often referred to as a 1264-62-6 Certificate of Suitability (COS). The purpose of a 1264-62-6 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of 1264-62-6 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of 1264-62-6 to their clients by showing that a 1264-62-6 CEP has been issued for it. The manufacturer submits a 1264-62-6 CEP (COS) as part of the market authorization procedure, and it takes on the role of a 1264-62-6 CEP holder for the record. Additionally, the data presented in the 1264-62-6 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the 1264-62-6 DMF.
A 1264-62-6 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. 1264-62-6 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 1264-62-6 suppliers with CEP (COS) on PharmaCompass.
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