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PRODUCT DETAIL

LOGNIF 0,5 mg tvrdé kapsuly

Code 7104D
MA number 59/0101/21-S
Product Form: cps dur 30x1x0,5 mg (blis.OPA/Al/PVC/papier/PET/Al-jednotliv.dáv.)
MA Status: R - Valid Marketing Authorisation
Type of procedure: Decentralised
MAH, country: TEVA Pharmaceuticals Slovakia s.r.o., Slovakia
Therapeutic Class: 59 - IMMUNOPRAEPARATA
ATC:
L ANTINEOPLASTIC AND IMMUNOMODULATING AGENTS
L04 Immunosuppressants
L04A Immunosuppressants
L04AE Sphingosine 1-phosphate (S1P) receptor modulators
L04AE01 Fingolimod
Shelf life: 24
Route of admin.: Oral use
Prescription Status: Medicinal product subject to restricted medical prescription.
Legal basis: Article 10(1) generic application
MA issued: 01.04.2021
Validity: 01.04.2026
Pediatric indication: Yes
Pediatric posology: Yes
Pediatric warnings: Yes
PIL: PIL_LOGNIF 0,5 mg_cps dur_09.2021.pdf  
SPC: SPC_LOGNIF 0,5 mg tvrdé kapsuly_07.2024.pdf  
Safety feature Yes
Data update: 03.07.2024
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