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PRODUCT DETAIL

Teriflunomide Glenmark 14 mg

Code 7046E
MA number 59/0243/23-S
Product Form: tbl flm 98x14 mg (blis.Al/Al)
MA Status: R - Valid Marketing Authorisation
Type of procedure: Decentralised
MAH, country: Glenmark Pharmaceuticals s.r.o., Czechia
Therapeutic Class: 59 - IMMUNOPRAEPARATA
ATC:
L ANTINEOPLASTIC AND IMMUNOMODULATING AGENTS
L04 Immunosuppressants
L04A Immunosuppressants
L04AK Dihydroorotate dehydrogenase (DHODH) inhibitors
L04AK02 Teriflunomide
Shelf life: 24
Container: blister Al/Al
Route of admin.: Oral use
Prescription Status: Medicinal product subject to restricted medical prescription.
Legal basis: Article 10(1) generic application
MA issued: 25.10.2023
Validity: 25.10.2028
Pediatric indication: Yes
Pediatric posology: Yes
Pediatric warnings: Yes
SPC: SPC_Teriflunomide Glenmark 14 mg_08.2024.pdf  
PIL: PIL_Teriflunomide Glenmark 14 mg_08.2024.pdf  
Dokument: Teriflunomid_Karta pre pacienta.pdf  
Dokument: Teriflunomid_Pokyny pre zdravotníckych pracovníkov.pdf  
Safety feature Yes
Data update: 09.08.2024
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