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Status : Withdrawn by Holder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Status : Withdrawn by EDQM Failure to CEP pro...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
98
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A MolPort-003-666-180 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MolPort-003-666-180, including repackagers and relabelers. The FDA regulates MolPort-003-666-180 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MolPort-003-666-180 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 MolPort-003-666-180 supplier is an individual or a company that provides MolPort-003-666-180 active pharmaceutical ingredient (API) or MolPort-003-666-180 finished formulations upon request. The MolPort-003-666-180 suppliers may include MolPort-003-666-180 API manufacturers, exporters, distributors and traders.
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A MolPort-003-666-180 CEP of the European Pharmacopoeia monograph is often referred to as a MolPort-003-666-180 Certificate of Suitability (COS). The purpose of a MolPort-003-666-180 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of MolPort-003-666-180 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of MolPort-003-666-180 to their clients by showing that a MolPort-003-666-180 CEP has been issued for it. The manufacturer submits a MolPort-003-666-180 CEP (COS) as part of the market authorization procedure, and it takes on the role of a MolPort-003-666-180 CEP holder for the record. Additionally, the data presented in the MolPort-003-666-180 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the MolPort-003-666-180 DMF.
A MolPort-003-666-180 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. MolPort-003-666-180 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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