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PRODUCT DETAIL

Brinsupri 25 mg filmom obalené tablety

Code 1953F
MA number EU/1/25/1995/001
Product Form: tbl flm 28 (2x14)x25 mg (blis.PVC/PCTFE/Al)
MA Status: E - Valid centralised marketing authorisation
Type of procedure: EU
MAH, country: Insmed Netherlands B.V., Netherland
Shelf life: 18
Container: blister PVC/PCTFE/Al
Route of admin.: Oral use
Prescription Status: Medicinal product subject to medical prescription.
Legal basis: Article 8(3) application - new active substance
MA issued: 18.11.2025
Validity: 18.11.2030
SmPC + PL: European Medicines Agency's database
Safety feature Yes
Data update: 21.11.2025
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