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01 1Boehringer Ingelheim Pharma GmbH & Co. KG Ingelheim Am Rhein DE
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01 1Etilefrine Hydrochloride
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01 1Germany
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01 1Valid
Certificate Number : R1-CEP 2000-011 - Rev 01
Status : Valid
Issue Date : 2006-04-26
Type : Chemical
Substance Number : 1205
71
PharmaCompass offers a list of Etilefrine 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 Etilefrine manufacturer or Etilefrine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Etilefrine manufacturer or Etilefrine supplier.
PharmaCompass also assists you with knowing the Etilefrine API Price utilized in the formulation of products. Etilefrine API Price is not always fixed or binding as the Etilefrine Price is obtained through a variety of data sources. The Etilefrine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Effontil manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Effontil, including repackagers and relabelers. The FDA regulates Effontil manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Effontil 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 Effontil manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Effontil supplier is an individual or a company that provides Effontil active pharmaceutical ingredient (API) or Effontil finished formulations upon request. The Effontil suppliers may include Effontil API manufacturers, exporters, distributors and traders.
click here to find a list of Effontil suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Effontil CEP of the European Pharmacopoeia monograph is often referred to as a Effontil Certificate of Suitability (COS). The purpose of a Effontil CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Effontil EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Effontil to their clients by showing that a Effontil CEP has been issued for it. The manufacturer submits a Effontil CEP (COS) as part of the market authorization procedure, and it takes on the role of a Effontil CEP holder for the record. Additionally, the data presented in the Effontil CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Effontil DMF.
A Effontil CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Effontil 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 Effontil suppliers with CEP (COS) on PharmaCompass.
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