01 1AbbVie Inc. North Chicago US
02 1SM BIOMED SDN BHD Sungai Petani MY
01 2Erythromycin stearate
01 1Malaysia
02 1U.S.A
01 1Valid
02 1Withdrawn by EDQM Failure to CEP procedure
Certificate Number : R1-CEP 1999-120 - Rev 03
Status : Valid
Issue Date : 2023-03-08
Type : Chemical
Substance Number : 490
Certificate Number : R1-CEP 2002-233 - Rev 01
Status : Withdrawn by EDQM Failure to CEP pro...
Issue Date : 2013-01-30
Type : Chemical and TSE
Substance Number : 490
87
PharmaCompass offers a list of Erythromycin Stearate 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 Stearate manufacturer or Erythromycin Stearate supplier for your needs.
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PharmaCompass also assists you with knowing the Erythromycin Stearate API Price utilized in the formulation of products. Erythromycin Stearate API Price is not always fixed or binding as the Erythromycin Stearate Price is obtained through a variety of data sources. The Erythromycin Stearate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A gallimycin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of gallimycin, including repackagers and relabelers. The FDA regulates gallimycin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. gallimycin 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 gallimycin supplier is an individual or a company that provides gallimycin active pharmaceutical ingredient (API) or gallimycin finished formulations upon request. The gallimycin suppliers may include gallimycin API manufacturers, exporters, distributors and traders.
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A gallimycin CEP of the European Pharmacopoeia monograph is often referred to as a gallimycin Certificate of Suitability (COS). The purpose of a gallimycin CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of gallimycin EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of gallimycin to their clients by showing that a gallimycin CEP has been issued for it. The manufacturer submits a gallimycin CEP (COS) as part of the market authorization procedure, and it takes on the role of a gallimycin CEP holder for the record. Additionally, the data presented in the gallimycin CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the gallimycin DMF.
A gallimycin CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. gallimycin 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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