Veranova: A CDMO that manages complexity with confidence.
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01 1MACFARLAN SMITH LIMITED Edinburgh GB
02 1ALKALOIDA CHEMICAL COMPANY ZRT. Tiszavasvari HU
03 1S.A.L.A.R.S. S.p.A. Como IT
04 1SANECA PHARMACEUTICALS A.S. Hlohovec SK
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01 4Dihydrocodeine hydrogen tartrate
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01 1Hungary
02 1Slovakia
03 1U.S.A
04 1United Kingdom
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01 4Valid
Dihydrocodeine Hydrogen Tartrate
Certificate Number : R1-CEP 2003-209 - Rev 01
Status : Valid
Issue Date : 2015-02-13
Type : Chemical
Substance Number : 1776
Dihydrocodeine Hydrogen Tartrate
Certificate Number : R1-CEP 2009-225 - Rev 02
Status : Valid
Issue Date : 2020-08-21
Type : Chemical
Substance Number : 1776
Dihydrocodeine Hydrogen Tartrate
Certificate Number : R1-CEP 2004-187 - Rev 01
Status : Valid
Issue Date : 2011-04-08
Type : Chemical
Substance Number : 1776
Dihydrocodeine Hydrogen Tartrate
Certificate Number : R1-CEP 2008-018 - Rev 01
Status : Valid
Issue Date : 2021-07-07
Type : Chemical
Substance Number : 1776
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PharmaCompass offers a list of Dihydrocodeine Tartrate 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 Dihydrocodeine Tartrate manufacturer or Dihydrocodeine Tartrate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Dihydrocodeine Tartrate manufacturer or Dihydrocodeine Tartrate supplier.
PharmaCompass also assists you with knowing the Dihydrocodeine Tartrate API Price utilized in the formulation of products. Dihydrocodeine Tartrate API Price is not always fixed or binding as the Dihydrocodeine Tartrate Price is obtained through a variety of data sources. The Dihydrocodeine Tartrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A DF 118 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DF 118, including repackagers and relabelers. The FDA regulates DF 118 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DF 118 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 DF 118 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A DF 118 supplier is an individual or a company that provides DF 118 active pharmaceutical ingredient (API) or DF 118 finished formulations upon request. The DF 118 suppliers may include DF 118 API manufacturers, exporters, distributors and traders.
click here to find a list of DF 118 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A DF 118 CEP of the European Pharmacopoeia monograph is often referred to as a DF 118 Certificate of Suitability (COS). The purpose of a DF 118 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of DF 118 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of DF 118 to their clients by showing that a DF 118 CEP has been issued for it. The manufacturer submits a DF 118 CEP (COS) as part of the market authorization procedure, and it takes on the role of a DF 118 CEP holder for the record. Additionally, the data presented in the DF 118 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the DF 118 DMF.
A DF 118 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. DF 118 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 DF 118 suppliers with CEP (COS) on PharmaCompass.
We have 4 companies offering DF 118
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