This HTML5 document contains 185 embedded RDF statements represented using HTML+Microdata notation.

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Namespace Prefixes

PrefixIRI
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n2http://linked.opendata.cz/resource/sukl/medicinal-product-packaging/
dctermshttp://purl.org/dc/terms/
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n3http://linked.opendata.cz/ontology/sukl/
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skoshttp://www.w3.org/2004/02/skos/core#
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n17http://www.ema.europa.eu/docs/cs_CZ/document_library/EPAR_-_Product_Information/human/001107/
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rdfhttp://www.w3.org/1999/02/22-rdf-syntax-ns#
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xsdhhttp://www.w3.org/2001/XMLSchema#
n6http://linked.opendata.cz/resource/sukl/medicinal-product-packaging/0167356/reimbursement/
n16http://linked.opendata.cz/resource/atc/
n9http://linked.opendata.cz/resource/sukl/df/

Statements

Subject Item
n2:0167356
rdf:type
n3:MedicinalProductPackaging
dcterms:title
DOCETAXEL TEVA 20 MG/0,72 ML
skos:notation
0167356
n3:hasATCCode
n16:L01CD02
n3:hasActiveIngredient
n13:DOCETAXELUM
n3:hasDefinedDailyDose
n4:ddd
n3:hasDosageForm
n9:INF-CSL-LQF-IVN
n3:hasPackagingSize
1X0.72ML+1X1.28ML SOLV
n3:hasPacking
n5:VIA
n3:hasRegistrationHolder
n20:TEVNL
n3:hasRegistrationState
n14:R
n3:hasRouteOfAdministration
n19:IVN
n3:hasStrength
27.73MG/ML
n3:hasIndicationGroup
n11:44
n3:hasSpecializationRestriction
n15:ONK
n3:containsDefinedDailyDoses
0.0
n3:hasRegistrationCode
EU/1/09/611/001
n3:hasTitleSupplement
INF CSL LQF 1X0.72ML+1X1.28ML
n3:containsUsualTherapeuticalDailyDoses
3.2362 3.237
n3:hasCoreReimbursementSpecification
n7:2015-07-01 n7:2015-07-02 n7:2015-02-01 n7:2015-03-01 n7:2015-01-01 n7:2015-01-13 n7:2015-05-01 n7:2015-06-01 n7:2015-04-01 n7:2015-04-02 n7:2013-08-01 n7:2013-08-03 n7:2013-06-01 n7:2013-07-01 n7:2013-11-01 n7:2013-12-01 n7:2013-09-01 n7:2013-10-01 n7:2013-01-01 n7:2013-01-05 n7:2013-04-01 n7:2013-05-01 n7:2013-02-01 n7:2013-03-01 n7:2014-09-01 n7:2014-10-01 n7:2014-07-03 n7:2014-08-01 n7:2014-11-19 n7:2014-12-01 n7:2014-10-02 n7:2014-11-01 n7:2014-03-01 n7:2014-04-01 n7:2014-01-01 n7:2014-02-01 n7:2014-06-13 n7:2014-07-01 n7:2014-05-01 n7:2014-06-01
n3:hasIndicationRestriction
P
n3:hasPriceOfOriginatorSpecification
n10:2015-07-01 n10:2015-07-02 n10:2014-11-19 n10:2014-12-01 n10:2014-10-02 n10:2014-11-01 n10:2014-09-01 n10:2014-10-01 n10:2014-07-03 n10:2014-08-01 n10:2015-05-01 n10:2015-06-01 n10:2015-04-01 n10:2015-04-02 n10:2015-02-01 n10:2015-03-01 n10:2015-01-01 n10:2015-01-13 n10:2013-11-01 n10:2013-12-01 n10:2013-09-01 n10:2013-10-01 n10:2013-08-01 n10:2013-08-03 n10:2013-06-01 n10:2013-07-01 n10:2014-06-13 n10:2014-07-01 n10:2014-05-01 n10:2014-06-01 n10:2014-03-01 n10:2014-04-01 n10:2014-01-01 n10:2014-02-01 n10:2013-04-01 n10:2013-05-01 n10:2013-02-01 n10:2013-03-01 n10:2013-01-01 n10:2013-01-05
n3:hasPriceSpecification
n8:2015-01-01 n8:2015-01-13 n8:2015-02-01 n8:2015-03-01 n8:2015-04-01 n8:2015-04-02 n8:2015-05-01 n8:2015-06-01 n8:2015-07-01 n8:2015-07-02 n8:2014-01-01 n8:2014-02-01 n8:2014-03-01 n8:2014-04-01 n8:2014-05-01 n8:2014-06-01 n8:2014-06-13 n8:2014-07-01 n8:2014-07-03 n8:2014-08-01 n8:2014-09-01 n8:2014-10-01 n8:2014-10-02 n8:2014-11-01 n8:2014-11-19 n8:2014-12-01 n8:2013-01-01 n8:2013-01-05 n8:2013-02-01 n8:2013-03-01 n8:2013-04-01 n8:2013-05-01 n8:2013-06-01 n8:2013-07-01 n8:2013-08-01 n8:2013-08-03 n8:2013-09-01 n8:2013-10-01 n8:2013-11-01 n8:2013-12-01
n3:hasReimbursementSpecification
n6:2014-09-01 n6:2014-10-01 n6:2014-07-03 n6:2014-08-01 n6:2014-11-19 n6:2014-12-01 n6:2014-10-02 n6:2014-11-01 n6:2015-02-01 n6:2015-03-01 n6:2015-01-01 n6:2015-01-13 n6:2015-05-01 n6:2015-06-01 n6:2015-04-01 n6:2015-04-02 n6:2013-08-01 n6:2013-08-03 n6:2013-06-01 n6:2013-07-01 n6:2013-11-01 n6:2013-12-01 n6:2013-09-01 n6:2013-10-01 n6:2014-03-01 n6:2014-04-01 n6:2014-01-01 n6:2014-02-01 n6:2014-06-13 n6:2014-07-01 n6:2014-05-01 n6:2014-06-01 n6:2013-01-01 n6:2013-01-05 n6:2013-04-01 n6:2013-05-01 n6:2013-02-01 n6:2013-03-01 n6:2015-07-01 n6:2015-07-02
n3:hasResumedMarketingDate
2010-12-01+01:00
n3:hasUsualTherapeuticalDailyDose
n4:utdd
n3:spcFile
http%3A%2F%2Fwww.ema.europa.eu%2Fdocs%2Fcs_CZ%2Fdocument_library%2FEPAR_-_Product_Information%2Fhuman%2F001107%2FWC500073419.pdf
n3:spcUri
n17:WC500073419.pdf