This HTML5 document contains 94 embedded RDF statements represented using HTML+Microdata notation.

The embedded RDF content will be recognized by any processor of HTML5 Microdata.

Namespace Prefixes

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n2	http://linked.opendata.cz/resource/sukl/medicinal-product-packaging/
dcterms	http://purl.org/dc/terms/
n4	http://linked.opendata.cz/resource/sukl/medicinal-product-packaging/0029180/reimbursement/
n3	http://linked.opendata.cz/ontology/sukl/
n13	http://linked.opendata.cz/resource/sukl/medicinal-product-packaging/0029180/
n7	http://linked.opendata.cz/resource/sukl/medicinal-product-packaging/0029180/core-reimbursement/
skos	http://www.w3.org/2004/02/skos/core#
n6	http://linked.opendata.cz/resource/sukl/medicinal-product-packaging/0029180/price/
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rdf	http://www.w3.org/1999/02/22-rdf-syntax-ns#
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xsdh	http://www.w3.org/2001/XMLSchema#
n17	http://linked.opendata.cz/resource/sukl/df/
n10	http://linked.opendata.cz/resource/atc/

Statements

Subject Item

n2:0029180

rdf:type

n3:MedicinalProductPackaging

dcterms:title

OPTIMARK 500 MIKROMOL/ML

skos:notation

0029180

n3:hasATCCode

n10:V08CA06

n3:hasActiveIngredient

n18:GADOVERSETAMIDUM

n3:hasDefinedDailyDose

n13:ddd

n3:hasDosageForm

n17:INJ-SOL-ISP-IVN

n3:hasPackagingSize

10X20ML

n3:hasPacking

n8:ISP

n3:hasRegistrationHolder

n16:MALD

n3:hasRegistrationState

n9:R

n3:hasRouteOfAdministration

n14:IVN

n3:hasStrength

500RM/ML

n3:hasIndicationGroup

n5:48

n3:hasSpecializationRestriction

n20:blank-cell

n3:containsDefinedDailyDoses

0.0

n3:hasRegistrationCode

EU/1/07/398/012

n3:hasTitleSupplement

IVN INJ SOL ISP 10X20ML

n3:containsUsualTherapeuticalDailyDoses

13.3333

n3:hasCoreReimbursementSpecification

n7:2013-10-01 n7:2013-11-01 n7:2013-08-03 n7:2013-09-01 n7:2014-02-01 n7:2014-03-01 n7:2013-12-01 n7:2014-01-01 n7:2014-04-01 n7:2013-01-01 n7:2013-03-01 n7:2013-04-01 n7:2013-01-05 n7:2013-02-01 n7:2013-07-01 n7:2013-08-01 n7:2013-05-01 n7:2013-06-01

n3:hasPriceOfOriginatorSpecification

n19:2014-04-01 n19:2014-02-01 n19:2014-03-01 n19:2013-12-01 n19:2014-01-01 n19:2013-10-01 n19:2013-05-01 n19:2013-11-01 n19:2013-06-01 n19:2013-08-03 n19:2013-03-01 n19:2013-09-01 n19:2013-07-01 n19:2013-04-01 n19:2013-01-05 n19:2013-08-01 n19:2013-02-01 n19:2013-01-01

n3:hasPriceSpecification

n6:2013-05-01 n6:2013-06-01 n6:2013-07-01 n6:2013-08-01 n6:2013-08-03 n6:2013-09-01 n6:2013-10-01 n6:2013-11-01 n6:2013-01-01 n6:2013-01-05 n6:2013-02-01 n6:2013-03-01 n6:2013-04-01 n6:2013-12-01 n6:2014-01-01 n6:2014-02-01 n6:2014-03-01 n6:2014-04-01

n3:hasReimbursementSpecification

n4:2013-02-01 n4:2013-01-01 n4:2013-12-01 n4:2014-01-01 n4:2013-10-01 n4:2013-11-01 n4:2014-04-01 n4:2014-02-01 n4:2014-03-01 n4:2013-05-01 n4:2013-06-01 n4:2013-03-01 n4:2013-04-01 n4:2013-08-03 n4:2013-09-01 n4:2013-07-01 n4:2013-08-01 n4:2013-01-05

n3:hasUsualTherapeuticalDailyDose

n13:utdd

n3:spcFile

http%3A%2F%2Fwww.emea.europa.eu%2Fdocs%2Fcs_CZ%2Fdocument_library%2FEPAR_-_Product_Information%2Fhuman%2F000745%2FWC500047540.pdf

n3:spcUri

n12:WC500047540.pdf