EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
01 1EUROAPI HUNGARY Ltd. Budapest HU
02 2DIPHARMA FRANCIS S.R.L. Baranzate IT
03 1SIEGFRIED LTD Zofingen CH
04 1SIEGFRIED PHARMACHEMIKALIEN MINDEN GMBH Minden DE
01 3Selegiline hydrochloride
02 1Selegiline hydrochloride, Helos 10%, Helos 50% and Helos 90%
03 1Selegiline hydrochloride, S2
01 1France
02 2Italy
03 2Switzerland
01 4Valid
02 1Withdrawn by Holder
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
Certificate Number : R1-CEP 1998-014 - Rev 04
Status : Valid
Issue Date : 2021-12-14
Type : Chemical
Substance Number : 1260
Certificate Number : R0-CEP 2023-056 - Rev 00
Status : Valid
Issue Date : 2023-04-20
Type : Chemical
Substance Number : 1260
Certificate Number : R1-CEP 2001-075 - Rev 03
Status : Valid
Issue Date : 2013-05-03
Type : Chemical
Substance Number : 1260
Certificate Number : R1-CEP 1999-124 - Rev 04
Status : Valid
Issue Date : 2015-12-15
Type : Chemical
Substance Number : 1260
Selegiline Hydrochloride, Helos 10%, Helos 50% A...
Certificate Number : R1-CEP 2005-272 - Rev 01
Status : Withdrawn by Holder
Issue Date : 2012-07-06
Type : Chemical
Substance Number : 1260
A Selegiline manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Selegiline, including repackagers and relabelers. The FDA regulates Selegiline manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Selegiline 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 Selegiline manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Selegiline supplier is an individual or a company that provides Selegiline active pharmaceutical ingredient (API) or Selegiline finished formulations upon request. The Selegiline suppliers may include Selegiline API manufacturers, exporters, distributors and traders.
click here to find a list of Selegiline suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Selegiline CEP of the European Pharmacopoeia monograph is often referred to as a Selegiline Certificate of Suitability (COS). The purpose of a Selegiline CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Selegiline EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Selegiline to their clients by showing that a Selegiline CEP has been issued for it. The manufacturer submits a Selegiline CEP (COS) as part of the market authorization procedure, and it takes on the role of a Selegiline CEP holder for the record. Additionally, the data presented in the Selegiline CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Selegiline DMF.
A Selegiline CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Selegiline 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 Selegiline suppliers with CEP (COS) on PharmaCompass.
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