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PRODUCT DETAIL

OPTISON 0,19 mg/ml injekčná disperzia

Code 46112
MA number EU/1/98/065/002
Product Form: dis inj 5x3 ml (liek.inj.skl.)
MA Status: E - Valid centralised marketing authorisation
Type of procedure: EU
MAH, country: GE Healthcare AS, Norway
Therapeutic Class: 48 - DIAGNOSTICA
ATC:
V VARIOUS
V08 CONTRAST MEDIA
V08D ULTRASOUND CONTRAST MEDIA
V08DA Ultrasound contrast media
V08DA01 Microspheres of human albumin
Shelf life: 24
Container: glass container
Route of admin.: Intravenous use
Prescription Status: Medicinal product subject to restricted medical prescription.
Legal basis: Article 8(3) application
MA issued: 18.05.1998
SmPC + PL: European Medicines Agency's database
Safety feature No
Data update: 28.10.2019
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