01 1AREVIPHARMA GMBH Radebeul DE
02 1EXCELLA GMBH & CO. KG Feucht DE
03 1LANDEN PHARMACHEM NV Landen BE
04 1SIEGFRIED PHARMACHEMIKALIEN MINDEN GMBH Minden DE
01 4Tilidine hydrochloride hemihydrate
01 1Belgium
02 2Germany
03 1Switzerland
01 1Expired
02 3Valid
Tilidine Hydrochloride Hemihydrate
Certificate Number : CEP 2006-013 - Rev 03
Status : Valid
Issue Date : 2025-01-21
Type : Chemical
Substance Number : 1767
Tilidine Hydrochloride Hemihydrate
Certificate Number : R0-CEP 2008-260 - Rev 01
Status : Expired
Issue Date : 2011-04-20
Type : Chemical
Substance Number : 1767
Tilidine Hydrochloride Hemihydrate
Certificate Number : R1-CEP 2007-045 - Rev 05
Status : Valid
Issue Date : 2023-02-16
Type : Chemical
Substance Number : 1767
Tilidine Hydrochloride Hemihydrate
Certificate Number : R1-CEP 2013-169 - Rev 00
Status : Valid
Issue Date : 2020-05-18
Type : Chemical
Substance Number : 1767
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PharmaCompass offers a list of Tilidine 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 Tilidine manufacturer or Tilidine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Tilidine manufacturer or Tilidine supplier.
PharmaCompass also assists you with knowing the Tilidine API Price utilized in the formulation of products. Tilidine API Price is not always fixed or binding as the Tilidine Price is obtained through a variety of data sources. The Tilidine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Tilidine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tilidine, including repackagers and relabelers. The FDA regulates Tilidine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tilidine API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Tilidine supplier is an individual or a company that provides Tilidine active pharmaceutical ingredient (API) or Tilidine finished formulations upon request. The Tilidine suppliers may include Tilidine API manufacturers, exporters, distributors and traders.
click here to find a list of Tilidine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Tilidine CEP of the European Pharmacopoeia monograph is often referred to as a Tilidine Certificate of Suitability (COS). The purpose of a Tilidine CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Tilidine EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Tilidine to their clients by showing that a Tilidine CEP has been issued for it. The manufacturer submits a Tilidine CEP (COS) as part of the market authorization procedure, and it takes on the role of a Tilidine CEP holder for the record. Additionally, the data presented in the Tilidine CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Tilidine DMF.
A Tilidine CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Tilidine 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 Tilidine suppliers with CEP (COS) on PharmaCompass.
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