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 Valerone manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Valerone, including repackagers and relabelers. The FDA regulates Valerone manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Valerone 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 Valerone supplier is an individual or a company that provides Valerone active pharmaceutical ingredient (API) or Valerone finished formulations upon request. The Valerone suppliers may include Valerone API manufacturers, exporters, distributors and traders.
click here to find a list of Valerone suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Valerone CEP of the European Pharmacopoeia monograph is often referred to as a Valerone Certificate of Suitability (COS). The purpose of a Valerone CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Valerone EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Valerone to their clients by showing that a Valerone CEP has been issued for it. The manufacturer submits a Valerone CEP (COS) as part of the market authorization procedure, and it takes on the role of a Valerone CEP holder for the record. Additionally, the data presented in the Valerone CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Valerone DMF.
A Valerone CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Valerone 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 Valerone suppliers with CEP (COS) on PharmaCompass.
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