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Status : Withdrawn by EDQM Failure to CEP pro...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Status : Withdrawn by Holder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