Veranova: A CDMO that manages complexity with confidence.
01 1MACFARLAN SMITH LIMITED Edinburgh GB
02 1FRANCOPIA Paris FR
03 1ALCALIBER S.A.U. Madrid ES
04 1S.A.L.A.R.S. S.p.A. Como IT
05 1SANECA PHARMACEUTICALS A.S. Hlohovec SK
06 1SIEGFRIED AG Zofingen CH
Veranova: A CDMO that manages complexity with confidence.
Morphine Hemisulfate 2.5-hydrate
Certificate Number : CEP 2001-239 - Rev 07
Status : Valid
Issue Date : 2024-06-20
Type : Chemical
Substance Number : 1244
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
Morphine Hemisulfate 2.5-hydrate
Certificate Number : CEP 2000-126 - Rev 07
Status : Valid
Issue Date : 2024-04-26
Type : Chemical
Substance Number : 1244
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PharmaCompass offers a list of Morphine Sulfate 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 Morphine Sulfate manufacturer or Morphine Sulfate supplier for your needs.
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PharmaCompass also assists you with knowing the Morphine Sulfate API Price utilized in the formulation of products. Morphine Sulfate API Price is not always fixed or binding as the Morphine Sulfate Price is obtained through a variety of data sources. The Morphine Sulfate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A MORPHABOND ER manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MORPHABOND ER, including repackagers and relabelers. The FDA regulates MORPHABOND ER manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MORPHABOND ER API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A MORPHABOND ER supplier is an individual or a company that provides MORPHABOND ER active pharmaceutical ingredient (API) or MORPHABOND ER finished formulations upon request. The MORPHABOND ER suppliers may include MORPHABOND ER API manufacturers, exporters, distributors and traders.
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A MORPHABOND ER CEP of the European Pharmacopoeia monograph is often referred to as a MORPHABOND ER Certificate of Suitability (COS). The purpose of a MORPHABOND ER CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of MORPHABOND ER EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of MORPHABOND ER to their clients by showing that a MORPHABOND ER CEP has been issued for it. The manufacturer submits a MORPHABOND ER CEP (COS) as part of the market authorization procedure, and it takes on the role of a MORPHABOND ER CEP holder for the record. Additionally, the data presented in the MORPHABOND ER CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the MORPHABOND ER DMF.
A MORPHABOND ER CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. MORPHABOND ER CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
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We have 6 companies offering MORPHABOND ER
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