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Status : Withdrawn by EDQM Failure to CEP pro...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Status : Withdrawn by Holder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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PharmaCompass also assists you with knowing the Aminophylline API Price utilized in the formulation of products. Aminophylline API Price is not always fixed or binding as the Aminophylline Price is obtained through a variety of data sources. The Aminophylline Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Miofilin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Miofilin, including repackagers and relabelers. The FDA regulates Miofilin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Miofilin 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 Miofilin supplier is an individual or a company that provides Miofilin active pharmaceutical ingredient (API) or Miofilin finished formulations upon request. The Miofilin suppliers may include Miofilin API manufacturers, exporters, distributors and traders.
click here to find a list of Miofilin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Miofilin CEP of the European Pharmacopoeia monograph is often referred to as a Miofilin Certificate of Suitability (COS). The purpose of a Miofilin CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Miofilin EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Miofilin to their clients by showing that a Miofilin CEP has been issued for it. The manufacturer submits a Miofilin CEP (COS) as part of the market authorization procedure, and it takes on the role of a Miofilin CEP holder for the record. Additionally, the data presented in the Miofilin CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Miofilin DMF.
A Miofilin CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Miofilin 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 Miofilin suppliers with CEP (COS) on PharmaCompass.
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