EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
01 1EUROAPI HUNGARY Ltd. Budapest HU
02 1ANHUI BIOCHEM PHARMACEUTICAL CO., LTD. Fuyang CN
03 2DIPHARMA FRANCIS S.R.L. Baranzate IT
01 3Selegiline hydrochloride
02 1Selegiline hydrochloride, S2
01 1China
02 1France
03 2Italy
01 4Valid
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 : CEP 2024-459 - Rev 00
Status : Valid
Issue Date : 2025-09-12
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 : R0-CEP 2023-056 - Rev 00
Status : Valid
Issue Date : 2023-04-20
Type : Chemical
Substance Number : 1260
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PharmaCompass offers a list of Selegiline 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 Selegiline Hydrochloride manufacturer or Selegiline Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Selegiline Hydrochloride manufacturer or Selegiline Hydrochloride supplier.
PharmaCompass also assists you with knowing the Selegiline Hydrochloride API Price utilized in the formulation of products. Selegiline Hydrochloride API Price is not always fixed or binding as the Selegiline Hydrochloride Price is obtained through a variety of data sources. The Selegiline Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Emsam manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Emsam, including repackagers and relabelers. The FDA regulates Emsam manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Emsam 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 Emsam manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Emsam supplier is an individual or a company that provides Emsam active pharmaceutical ingredient (API) or Emsam finished formulations upon request. The Emsam suppliers may include Emsam API manufacturers, exporters, distributors and traders.
click here to find a list of Emsam suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Emsam CEP of the European Pharmacopoeia monograph is often referred to as a Emsam Certificate of Suitability (COS). The purpose of a Emsam CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Emsam EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Emsam to their clients by showing that a Emsam CEP has been issued for it. The manufacturer submits a Emsam CEP (COS) as part of the market authorization procedure, and it takes on the role of a Emsam CEP holder for the record. Additionally, the data presented in the Emsam CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Emsam DMF.
A Emsam CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Emsam 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 Emsam suppliers with CEP (COS) on PharmaCompass.
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