Medicinal Products

Lenalidomid Teva 10 mg tvrde kapsule

Name Lenalidomid Teva 10 mg tvrde kapsule
Marketing Authorisation Number HR-H-696999362
Active Substance lenalidomidum
Pharmaceutical Form kapsula, tvrda
Strength 10 mg
Packaging [MA Number for Packaging] 7 kapsula u blisteru, u kutiji  [HR-H-696999362-01]
7 kapsula u blisteru s jediničnom dozom, u kutiji  [HR-H-696999362-02]
21 kapsula u blisteru, u kutiji  [HR-H-696999362-03]
21 kapsula u blisteru s jediničnom dozom, u kutiji  [HR-H-696999362-04]
Manufacturer Teva UK Ltd., Eastbourne, East Sussex, Ujedinjeno Kraljevstvo;
Pliva Hrvatska d.o.o., Zagreb, Republika Hrvatska;
Merckle GmbH, Blaubeuren, Baden-Wuerttemberg, Njemačka;
Teva Pharma B.V., Haarlem, Nizozemska;
Teva Operations Poland Sp. z o.o., Krakow, Poljska
Marketing Authorisation Holder Teva B.V., Swensweg 5, Haarlem, Nizozemska
Marketing Authorisation Date 27.07.2018
MA Period of Validity 27.07.2023
Classification Number UP/I-530-09/17-01/174
Registration Number 381-12-01/30-18-03
Composition jedna kapsula sadrži lenalidomidklorid hidrat što odgovara 10 mg lenalidomida
Prescription na recept
Type of prescription ograničeni recept
Distribution u ljekarni
Advertising to general public zabranjeno
ATC Code L04AX04
Medicinal product marketed in the Croatia Da
SmPC download
PL download
Public Assessment Report download
Educational materials
for healthcare professionals
Vodič za zdravstvene radnike, verzija 3
Kontrolni popis za propisivače, verzija 2
Obrazac za prijavu trudnoće, verzija 2
Obrazac pristanka bolesnika, verzija 2
Educational materials
for patients / caregivers
Vodič za bolesnike, verzija 3
Kartica za bolesnika, verzija 2
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