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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
01 4Dihydrocodeine hydrogen tartrate
01 1Hungary
02 1Slovakia
03 1U.S.A
04 1United Kingdom
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
A Dihidrocodeina manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dihidrocodeina, including repackagers and relabelers. The FDA regulates Dihidrocodeina manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dihidrocodeina 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 Dihidrocodeina manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Dihidrocodeina supplier is an individual or a company that provides Dihidrocodeina active pharmaceutical ingredient (API) or Dihidrocodeina finished formulations upon request. The Dihidrocodeina suppliers may include Dihidrocodeina API manufacturers, exporters, distributors and traders.
click here to find a list of Dihidrocodeina suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Dihidrocodeina CEP of the European Pharmacopoeia monograph is often referred to as a Dihidrocodeina Certificate of Suitability (COS). The purpose of a Dihidrocodeina CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Dihidrocodeina EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Dihidrocodeina to their clients by showing that a Dihidrocodeina CEP has been issued for it. The manufacturer submits a Dihidrocodeina CEP (COS) as part of the market authorization procedure, and it takes on the role of a Dihidrocodeina CEP holder for the record. Additionally, the data presented in the Dihidrocodeina CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Dihidrocodeina DMF.
A Dihidrocodeina CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Dihidrocodeina 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 Dihidrocodeina suppliers with CEP (COS) on PharmaCompass.
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