01 1CSPC INNOVATION PHARMACEUTICAL CO., LTD. Shijiazhuang City CN
02 1Jilin Shulan Synthetic Pharmaceutical Co. Ltd. Shulan City CN
03 2SIEGFRIED PHARMACHEMIKALIEN MINDEN GMBH Minden DE
01 3Theophylline-ethylenediamine
02 1Theophylline-ethylenediamine hydrate
01 2China
02 2Switzerland
01 2Valid
02 1Withdrawn by EDQM Failure to CEP procedure
03 1Withdrawn by Holder
Certificate Number : R0-CEP 2007-345 - Rev 01
Status : Withdrawn by EDQM Failure to CEP pro...
Issue Date : 2010-02-09
Type : Chemical
Substance Number : 300
Certificate Number : R1-CEP 2004-140 - Rev 00
Status : Withdrawn by Holder
Issue Date : 2011-09-19
Type : Chemical
Substance Number : 300
Certificate Number : R1-CEP 2007-288 - Rev 01
Status : Valid
Issue Date : 2015-12-15
Type : Chemical
Substance Number : 300
Theophylline-ethylenediamine Hydrate
Certificate Number : R1-CEP 2007-289 - Rev 01
Status : Valid
Issue Date : 2015-12-15
Type : Chemical
Substance Number : 301
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PharmaCompass offers a list of Aminophylline 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 Aminophylline manufacturer or Aminophylline supplier for your needs.
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A Eufilina Venosa manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Eufilina Venosa, including repackagers and relabelers. The FDA regulates Eufilina Venosa manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Eufilina Venosa 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 Eufilina Venosa supplier is an individual or a company that provides Eufilina Venosa active pharmaceutical ingredient (API) or Eufilina Venosa finished formulations upon request. The Eufilina Venosa suppliers may include Eufilina Venosa API manufacturers, exporters, distributors and traders.
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A Eufilina Venosa CEP of the European Pharmacopoeia monograph is often referred to as a Eufilina Venosa Certificate of Suitability (COS). The purpose of a Eufilina Venosa CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Eufilina Venosa EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Eufilina Venosa to their clients by showing that a Eufilina Venosa CEP has been issued for it. The manufacturer submits a Eufilina Venosa CEP (COS) as part of the market authorization procedure, and it takes on the role of a Eufilina Venosa CEP holder for the record. Additionally, the data presented in the Eufilina Venosa CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Eufilina Venosa DMF.
A Eufilina Venosa CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Eufilina Venosa 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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