01 1ANUH PHARMA LTD. Mumbai IN
02 1AbbVie Inc. North Chicago US
03 1ERCROS S.A. Aranjuez ES
04 1SM BIOMED SDN BHD Sungai Petani MY
05 1Sandoz Industrial Products SpA Rovereto IT
01 3Erythromycin ethylsuccinate
02 1Erythromycin ethylsuccinate, Powder, micronised
03 1Erythromycin ethylsuccinate, Pulverised
01 1Germany
02 1India
03 1Malaysia
04 1Spain
05 1U.S.A
01 3Valid
02 1Withdrawn by EDQM Failure to CEP procedure
03 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Status : Withdrawn by Holder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
Certificate Number : R1-CEP 1999-138 - Rev 03
Status : Withdrawn by EDQM Failure to CEP pro...
Issue Date : 2012-12-14
Type : Chemical
Substance Number : 274
A Erythromycin Ethyl Succinate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Erythromycin Ethyl Succinate, including repackagers and relabelers. The FDA regulates Erythromycin Ethyl Succinate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Erythromycin Ethyl Succinate 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 Erythromycin Ethyl Succinate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Erythromycin Ethyl Succinate supplier is an individual or a company that provides Erythromycin Ethyl Succinate active pharmaceutical ingredient (API) or Erythromycin Ethyl Succinate finished formulations upon request. The Erythromycin Ethyl Succinate suppliers may include Erythromycin Ethyl Succinate API manufacturers, exporters, distributors and traders.
click here to find a list of Erythromycin Ethyl Succinate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Erythromycin Ethyl Succinate CEP of the European Pharmacopoeia monograph is often referred to as a Erythromycin Ethyl Succinate Certificate of Suitability (COS). The purpose of a Erythromycin Ethyl Succinate CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Erythromycin Ethyl Succinate EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Erythromycin Ethyl Succinate to their clients by showing that a Erythromycin Ethyl Succinate CEP has been issued for it. The manufacturer submits a Erythromycin Ethyl Succinate CEP (COS) as part of the market authorization procedure, and it takes on the role of a Erythromycin Ethyl Succinate CEP holder for the record. Additionally, the data presented in the Erythromycin Ethyl Succinate CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Erythromycin Ethyl Succinate DMF.
A Erythromycin Ethyl Succinate CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Erythromycin Ethyl Succinate 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 Erythromycin Ethyl Succinate suppliers with CEP (COS) on PharmaCompass.
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