01 1CHIFENG ARKER PHARMACEUTICAL TECHNOLOGY CO., LTD. Chifeng CN
02 1SIEGFRIED PHARMACHEMIKALIEN MINDEN GMBH Minden DE
03 1VUAB Pharma a.s. Roztoky CZ
04 1Xinjiang Heshuo Ephedrine Product Co., Ltd Urumqi CN
01 4Ephedrine hydrochloride
01 2China
02 1Czech Republic
03 1Switzerland
01 2Valid
02 1Withdrawn by EDQM Failure to CEP procedure
03 1Withdrawn by Holder
Certificate Number : R1-CEP 2002-193 - Rev 00
Status : Withdrawn by Holder
Issue Date : 2010-06-17
Type : Chemical
Substance Number : 487
Certificate Number : R1-CEP 2006-234 - Rev 01
Status : Valid
Issue Date : 2015-12-15
Type : Chemical
Substance Number : 487
Certificate Number : R1-CEP 2002-157 - Rev 00
Status : Valid
Issue Date : 2009-06-30
Type : Chemical
Substance Number : 487
Certificate Number : R0-CEP 2004-152 - Rev 00
Status : Withdrawn by EDQM Failure to CEP pro...
Issue Date : 2005-12-15
Type : Chemical
Substance Number : 487
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PharmaCompass offers a list of Ephedrine Hydrochloride 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 Ephedrine Hydrochloride manufacturer or Ephedrine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ephedrine Hydrochloride manufacturer or Ephedrine Hydrochloride supplier.
PharmaCompass also assists you with knowing the Ephedrine Hydrochloride API Price utilized in the formulation of products. Ephedrine Hydrochloride API Price is not always fixed or binding as the Ephedrine Hydrochloride Price is obtained through a variety of data sources. The Ephedrine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Altusin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Altusin, including repackagers and relabelers. The FDA regulates Altusin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Altusin API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Altusin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Altusin supplier is an individual or a company that provides Altusin active pharmaceutical ingredient (API) or Altusin finished formulations upon request. The Altusin suppliers may include Altusin API manufacturers, exporters, distributors and traders.
click here to find a list of Altusin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Altusin CEP of the European Pharmacopoeia monograph is often referred to as a Altusin Certificate of Suitability (COS). The purpose of a Altusin CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Altusin EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Altusin to their clients by showing that a Altusin CEP has been issued for it. The manufacturer submits a Altusin CEP (COS) as part of the market authorization procedure, and it takes on the role of a Altusin CEP holder for the record. Additionally, the data presented in the Altusin CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Altusin DMF.
A Altusin CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Altusin 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 Altusin suppliers with CEP (COS) on PharmaCompass.
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