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PRODUCT DETAIL

Herceptin 600 mg injekčný roztok v liekovke

Code 6957A
MA number EU/1/00/145/002
Product Form: sol inj 1x5 ml (liek.inj.skl.)
MA Status: E - Valid centralised marketing authorisation
Type of procedure: EU
MAH, country: Roche Registration GmbH, Germany
Therapeutic Class: 44 - CYTOSTATICA
ATC:
L ANTINEOPLASTIC AND IMMUNOMODULATING AGENTS
L01 ANTINEOPLASTIC AGENTS
L01F MONOCLONAL ANTIBODIES AND ANTIBODY DRUG CONJUGATES
L01FD HER2 (Human Epidermal Growth Factor Receptor 2) inhibitors
L01FD01 Trastuzumab
Shelf life: 21
Container: glass vial
Route of admin.: Subcutaneous use
Prescription Status: Medicinal product subject to restricted medical prescription.
Legal basis: Article 8(3) application
MA issued: 28.08.2000
SmPC + PL: European Medicines Agency's database
Dokument: DHPC Herceptin falšovanie 5 5 2014.pdf  
Safety feature Yes
Data update: 27.08.2024
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